Instructor's Portfolio

Dr. CRISTINA SKRYPNYK


Assistant Professor

College of Medicine and Medical Sciences
Work Tel No: 17237315 Work Fax No: 17246022
cristinas@agu.edu.bh



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Qualifications

Qualifications

- University of Medicine "G. T. Popa",Iasi,Romania/Medical Doctor/1990-1996
- Ministry of Health, Office of Professional Qualification Recognition Romania/ Specialist Physician in Medical Genetics/2004
- University of Medicine "G. T. Popa"Iasi, Romania,Human Genetics Unit/PhD title in Medical Sciences/2007
- Ministry of Health, Office of Professional Qualification Recognition Romania/Consultant Physician in Medical Genetics/2009
- Ministry of Education and Research, Ministry of Labor Romania/Project Manager/2009

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Work Experience

Experience

- Assistant Professor/Arabian Gulf University, College of Medical Sciences, Manama,Bahrain/since 09.2010
-Assistant Professor/University of Oradea, Faculty of Medicine,Genetics Department,Oradea,Romania/02.2002-10.2010
- University Preparer/University of Oradea, Faculty of Medicine,Genetics Department,Oradea,Romania/10.1998-01.2002

- Consultant Medical Genetics/Al Jawhara Center for Molecular Medicine, Manama, Bahrain/since 09.2010
- Consultant Medical Genetics/Clinical Municipal Hospital „Dr.G.Curteanu",Genetics Depart.,Oradea,Romania/10.2009-09.2010
- Specialist Medical Genetics/Clinical Municipal Hospital"Dr. G. Curteanu" Genetics Depart.,Oradea,Romania/03.2004–09.2009
- Resident physician in Medical Genetics/County Health Office,Oradea, Romania/04.1999-04.2004

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Scientific Production

Publication

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Teaching Courses

Teaching Courses

- PBL Tutor to Year 2 students, Unit II/III
- PBL Tutor to Year 3 students, Unit IV
- PBL Tutor to Year 4 students, Unit VII/VIII/IX
- Resource faculty for Year 2 students, Unit II / Year 4 students, Unit IX
- Academic advisor for Year 3 students
- PhD program in Molecular Medicine, courses: B1,B8

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Academic Supervision

Supervised the following theses

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Committees

 

Attendance in most important committees within the university

- Academic committee PhD in Molecular Medicine
- BSc Exam committee
- Advisory committees- academic advisor for Year 3
- NCAAA meetings- faculty group responsible for participating in community services; Standard 11.
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Memberships

 

- European Society of Human Genetics
- European Cytogeneticists Association
- Romanian Society of Medical Genetics
- Asia Pacific Society of Human Genetics
- American Society of Human Genetics
- Bahrain Medical Society
- International Federation of University Women
- International Conferences for Rare Diseases and Orphan Drugs
- Central and Eastern European Genetic Network
- Information Center for Rare Disorders Romania
- European Organization of Rare Disorders EURORDIS
- EuroGentest
- Rare Chromosomal Disorders Support Group
- Assistant editor of “Romanian Journal of Rare Diseases”
- Editorial committee member of Romanian medical review-“Stetoscop”
- Scientific referee of Romanian Medical Publishing Antaeus
- Scientific referee Romanian Review of Laboratory Medicine RRLM
- Scientific referee Journal of Translational Medicine
- Scientific referee Arab Gulf Journal of Scientific Research
- International Judge for the ESHG/ ASHG DNA-Day International Essay contest

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Community Service

 

- Rare Disease Public Campaign Bahrain, 28 February 2014, City Center Mall, organizing committee member and volunteer
- Rare Disease Public Campaign Bahrain, 29 February 2013, Seef Mall, organizing committee member and volunteer
- Ministry of Education, Visits of high schools students, 11-12 December 2012; 23- 24, 29- 30 April 2013- Lecture “The meaning of medical genetics and its contribution to the people health”.

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Research Interests

 

- genomic disorders
- rare disorders
- ethical aspects of genetic testing

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Lectures/Seminars/Workshops

 

Workshops:
- "Best Practice in Medical Genetics:genetic testing and ethical issues"- workshop,1st Gulf Medical Administration Forum, 6 June 2013, Manama, Bahrain
- "“Ethics and professionalism workshop”, Introduction to problem based learning, year II, College of Medicine, Arabian Gulf University, 6th September 2012,4 September 2013
-"Medical ethics workshop” Year IV, College of Medicine, Arabian Gulf University, 26 March 2013

Postgraduates training course:
-26th Course in Medical Genetics, 12-16 May 2013, webcasted from European School of Genetics Medicine, Bologna Italy at the Remote Training Center Al Jawhara Center for Molecular Medicine, Manama Bahrain; Remote Training Center Director

Oral presentations:
- "From human genes to disorders", Seminar for patients and their families, Al Jawhara Center Bahrain, 28 March 2014
- "ECARUCA - the online database for rare chromosome disorders", 5th Pan Arab Human Genetics Conference, Dubai, United Arab Emirates, 17-19 November 2013.
- "Prenatal genetic diagnosis", SMC Obstetrics and Gynecology Department, Continuing Education Program, 20 of June,2013
- "Rare Diseases impact into societies worldwide", Rare Disease Day Symposium 2013 Bahrain, 26 of February, Al Jawhara Center, Manama, Bahrain.
-" The meaning of medical genetics and its contribution to the people health", Highschool students visits to Al Jawhara Center, 9, 12 December 2012.
"Medical Genetics today", American Mission Hospital, The Continuing Medical Education Program- 4 July 2011, Manama, Bahrain
-"Genetics data bases-a guide for proper and sharp diagnosis",AlJawhara Center Journal Club, 2nd of June 2011
-"Rare genomic disorders", Journal Club, Anatomy Department, College of Medicine and Medical Sciences, Arabian Gulf University, 24 January 2011
-"Genomic disorders",Al Jawhara Center Journal Club,11 November 2010
-"Breast cancer- background and molecular diagnostic methods",Al-Jawhara Center Journal Club,7 October 2010
- “Genetics data base used in medical practice”. National Medical Genetics Conference, 24-26 Septembrie 2009, Sibiu, Romania
-"„The role of medical geneticist in the management team of rare disorders”,Balkan Congress for Rare Diseases Romania, 26-28 June 2009, Cluj Napoca, Romania.
- „Mechanisms and assays for rare genomic disorders”,Balkan Congress for Rare Diseases Romania, 26-28 June 2009, Cluj Napoca, Romania.
-“Genotype-phenotype correlation in Prader Willi syndrome- an overview of the literature”, 1st Eastern European Conference on PWS „Review Multidisciplinary approach in the management of PWS”, Timisoara, 24-25 April 2009.
- “Importance of an early and correct diagnosis for a correct genetic counseling", Diagnosis, treatment and management of rare diseases patients workshop, National Alliance for Rare Diseases, National Center for Family Medicine Studies, Bucharest, 28 February 2009.
- Diagnosis and therapy in Down Syndrome”, Oradea, 3 December 2008.
- International Pediatric Cardiology Symposium, 9-12 October 2008, Tg Mures, Romania
-"Early diagnosis of rare diseases”. Trust of trust- Hope and trust for rare disease patients", 24 September 2008, Cluj, Romania
- The 5th German-Romanian Genetics Course, 14-17 April 2008, Oradea, Romania
-“Beeckwith Wiedemann syndrome”, First Rare Disease European Day Symposium , Faculty of medicine and Pharmacy, 28 February 2008,Oradea, Romania
- „Light and shadows; diagnosing rare genetics disorders”, Rare disorders- finding the needs and establishing the priorities,Zal?u, 2-3 November, Romania
- „Diagnosis of microdeletion and microduplications syndromes, from karyotype to molecular genetics tests”,The 6th National Congress of Laboratory Medicine", 11-13 October, 2007, Sibiu, Romania
- „Importance of the minor criteria for a positive clinical diagnosis of Prader Willi syndrome patients", 6th International Prader-Willi Syndrome Scientific Conference, 1st Romanian Prader-Willi Syndrome and Rare Diseases Conference, 21-24 June 2007, Cluj-Napoca, Romania.
-"Genetics test across borders”, 6th International Prader-Willi Syndrome Scientific Conference, 1st Romanian Prader-Willi Syndrome and Rare Diseases Conference, 21-24 June 2007, Cluj-Napoca, Romania.
- “Molecular genetics contributions in the diagnosis of microdeletion and microduplication syndromes”. Romanian Society of Medical Genetics Conference, 25-27 May 2007, Moeciu de Sus, Brasov, Romania .
- „Beckwith Wiedemann syndrome-paternal UPD 11”. The 2nd Romanian Congress of Medical Genetics, 20-23 September 2006, Cluj, Romania

Posters:
-" Rare genetic diseases- Genetic counselling challenges". Cristina Skrypnyk. 10th Asia-Pacific Conference on Human Genetics
5th - 8th December 2012, Kuala Lumpur, Malaysia.
-„Cardiovascular spectrum in Williams Beuren syndrome”. C. Skrypnyk, M. Bembea, C. Jurca, C. Liveratou, D. Smeets. European Human Genetics Conference 23-26 May 2009, Vienna, Austria. In European Journal of Human genetics, Vol 17, Supplement 2, May 2009, pg 141.
-„From phenotype to mosaic paternal UPD11p15 in Beckwith Wiedeman Syndrome” C Skrypnyk, M. Bembea,V Bica, C. Rusu, C. Jurca, W. Kress, A. Baumer. European Human Genetics Conference 31 May-3 June 2008, Barcelona, Spain. In European Journal of Human genetics, Vol16, Supplement 2, p 133.
-„Screening for subtelomeric rearrangements by multiplex ligation-dependent probe amplification (MLPA) in 30 patients with mental retardation.” C. Skrypnyk, M. Bembea, C. Jurca, E. Neagu, D. Iancu, L. Barbarii, C. Rusu. Genomic Disorders 2008, Wellcome Trust Conference Centre, Hinxton, Cambridge, UK, 17-20 march 2008.
-“MLPA for the detection of cryptic subtelomeric rearrangements in mental retardation patients- cases report “. C. Skrypnyk, M. Bembea, C. Jurca, E. Neagu, D. Iancu, L. Barbarii, C. Rusu. 6th European Cytogenetics Conference, 7-10 July 2007, Istanbul, Turkey.
-„Williams Syndrome - observing the phenotype and understanding the genotype”. C. Skrypnyk, M. Bembea, C. Rusu, M. Volosciuc, M. Gramescu, M. Covic, D. Smeets, O. Bartsch. Genomic Disorders 2007, 21-24 March 2007, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK.
-„ Genetic counselling in microdeletions syndromes”. C. Skrypnyk, M. Bembea, V. Belengeanu, E. Tomescu, P. Grigorescu Sido, M. Covic. The 7th Course Genetic Counselling in Practice, European School of Genetic Medicine, November 9-14 2006, Bertinoro, Italy.
-„Prader-Willi Syndrome: clinical and molecular particular aspects” C. Skrypnyk, M. Bembea, O. Bartsch, C. Aulehla-Scholz, W. Kress . Second Eastern European Confererence on Rare Diseases and Orphan Drugs. Fostering Research on Rare Diseases in Eastern European Countries, 8-9 Septembrie 2006, Plovdiv, Bulgaria- in extenso, Conference proceedings ISBN978-954-91025-3-6, pg 179-180.
-„A particular case of syndromatic ichtyosis”. C. Skrypnyk, O. Bartsch, M. Bembea, V. Filip, I. I. Vancsik. European Conference of Human Genetics, Amsterdam, 6-9 May, 2006.
-„Hereditary multiple exostoses disease- clinical and genetical aspects”. C. Skrypnyk, M. Bembea, O. Vancsik, M. Barbu, C. Barbu. -European Conference of Human Genetics, Prague, 9-11 May, 2005.
-„Singular and syndromatic ano-rectal malformations“. C. Skrypnyk , M. Bembea, R. Spineanu, F. Galos, O. Vancsik, , C. Todor, D. Lerintiu- “The 10th International Congress of Human Genetics”:15-19 May 2001, Vienna, Austria.

Conferences attended:
- Advances In Neurogenetics Research "A collaborative Symposium" 21-22 March 2014, Doha, Qatar.
-“A walk through Forensic Medicine- 20-21 March 2014, Arabian Gulf University, Manama, Kingdom of Bahrain
- 11th Gulf Heart Association Joint With 4th Bahrain Heart Association Congress, 26-28 feb 2014, Manama, Bahrain
- 9th GCC Medical Education Conference”, 23-25 November 2013, Arabian Gulf University, Manama, Kingdom of Bahrain
- 5th Pan Arab Human Genetics Conference &Golden Helix Symposium, 17-19 Nov 2013, Dubai
-European Cytogenetic Association Conference, 28 June-2 Jul 2013 Dublin, Ireland
-First Gulf Forum for Medical Administration “Code of Ethics”, 4-6 June, Manama, Bahrain.
- 3rd GCC Symposium in Clinical Nutrition, 10-11 April, University Medical Center, King Abdullah Medical City, Bahrain
-First International Rheumatology Conference, 9th of March, King Hamad Hospital,Manama, Bahrain
- Dementia Symposium, 5th of March, 2013, Al Jawhara Center, Manama, Bahrain
- First International Diabetes Symposium, 2-3 March 2013, Arabian Gulf University, Baharain
-Rare Disease Day Symposium Bahrain 2013, 26 th of February 2013, Al Jawhara Center, Manama, Bahrain
- 10th Asia Pacific Conference in Human Genetics, 5-8 December 2012, Kuala Lumpur,Malaysia
-IUPS Physiology teaching Conferences and workshop, 31 March- 1 April 2012, Arabian Gulf, University, Manama, Bahrain
-8th International Conference, HH Princess Al Jawhara Centre for Molecular Medicine, Genetics and Inherited Disorders, 28-29 November 2011, Manama, Bahrain
- European Human Genetics Conference, 28-31 May 2011, Amsterdam, Holland
- Symposium „Array in daily practice: promises and pitfalls”, 27 May 20011, Amsterdam, Holland
- EUROPLAN Conference European Project of Rare Diseases National Plans Development,18-19 June 2010, Romanian Parliament, Bucharest, Romania.
- National Congress for Brest Cancer- present and future, Baile Felix 12-15 May 2010, Romania.
- Conference “OI in motion” Rehabilitation and Physiotherapy in Osteogenesis imperfecta, 20-22 November 2009, Rheinsberg, Germany.
- National Conference of Medical Genetics, 24-26 September 2009, Sibiu, Romania.
- Balkan Congress for Rare Diseases Romania, 26-28 June 2009, Cluj Napoca, Romania.
-European Human Genetics Conference 25-26 May, 2009, Vienna, Austria.
- 1st Eastern European Conference on PWS „Review Multidisciplinary approach in the management of PWS”, Timisoara, 24-25 April 2009.
- "How to diagnose, to treat and to manage the patients with rare disorders"- National Alliance for Rare Disorder, National Center for Family Medicine, Bucharest, 28 February 2009.
- „Diagnosis and therapy in Down syndrome”, 3 December 2008, Oradea, Romania.
- “National Strategies and Action Plans for Rare Diseases in Europe”, “State of the art and sharing experiences: towards EU Recommendations”, 18 November 2008, French Ministry of Health, Paris,France
-„EURORDIS- Conference of National Aliances”, 17 November, Rare Diseases Platform,Paris, France
- The third international symposium of Pediatric Cardiology , 9-12 October 2008, Tg Mures,Romania
-„Trust of Trust- hope and trust for patients with rare disorders”, 24 September, 2008, Cluj Napoca, Romania.
- European Human Genetics Conference 2008, 31May- 3 June, Barcelona, Spain
- Genomic Disorders 2008, 17-20 March,Wellcome Trust Genome,Cambridge
- „First European Day of Rare Disorders”- Symposium, 28 February 2008, Facutly of Medicine and Pharmacy, Oradea, Romania
- “Rare disorders- from needs to priorities”2-3 November 2007, Zalau, Romania
-Building Towards Profesional Competence and Patient Confidence, EuroGentest, October 27-28, 2007, Milan, Italy.
- The 6th National Congress with international participation of Laboratory Medicine, the 2nd Symposium of Immunopathology, 11-13 October 2007, Sibiu, Romania.
- 6th European Cytogenetics Conference, 7-10 July 2007, Istanbul Turkey.
- 6th International Prader-Willi Syndrome Scientific Conference, 1st Romanian Prader Willi Syndrome and Rare Diseases Conference, 21-24 June 2007, Cluj, Romania.
- National Conference of Medical Genetics, 25-27 May 2009, Moeciu de Sus, Romania.
- Genomic Disorders 2007, 21-23 March, Wellcome Trust Genome,Cambridge, UK.
-European Human Genetics Conference 2005, 6-9 May, Amsterdam, The Nederland.
- Second Eastern European Conference on Rare Diseases and Orphan Drugs, 8-9 September Plovdiv, Bulgaria
-Save PKU kids”, 29-30 September,Oradea, Romania.
- European Human Genetics Conference 2005, 7-10 May, Prague, Czech Republic.
-1st National Conference of Bioethics, Iasi, Romania.
-The 3rd National Symposium of genetics disorders, endocrine amd metabolic disorders in children ”, 12 June 2004, Cluj Napoca, Romania
- The International Congress of Mucoviscidosis, May 7-9 , Timisoara, Romania.
- International Congress of Perinatal Medicine, October 1-4, Cluj Napoca, Romania
-1st National Congress of Medical Genetics, 19-22 September Oradea, Romania
- The 10th International Congress of Human Genetics,May 15-19, Vienna
-100 Jahre Nobelpreis an Emil von Behring: 20 Oktober, 2001, Berlin, Germany
- International Symposium in Bioethics- 2nd edition :22-24 of June 2001, Oradea, Romania
- Scientific meeting Romania-Sweden: 23-24 February 2001, Oradea, Romania
- The 4th National Conference of Neonatolgy: 28-30 September 2000 Oradea, Romania
-The 1st Congress of The Anatomy Departments, The Medical Union of Balkans and Black Sea Region Countries : 2-4 June 2000 Oradea, Romania
-National Conference of Medical Genetics, 7-10 October 1999, Constanta, Romania
-The 3rd National Congress of Social Pediatry, 30 September- 2 October 1999, Romania
-Balkan Medical Days: 28-30 April 1999 Iasi, Romania

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Publications prior to joining AGU

 


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Others

 

Expertise:
Genetic diseases- evaluation, diagnosis, testing, management
Genetic counseling
Cytogenetics and Molecular Cytogenetics, Molecular Genetics

Cytogenetics and molecular genetics trainings:
- Genome Wide Array diagnostic technique: Division of Genome Diagnostics, Human Genetics Department, Radboud University Medical Center, Nijmegen, Holland,2013
-RT PCR, FISH techniques: GeneticLab, Bucharest, Romania, Molecular Department, 2008
-FISH technique: University of Medicine and Pharmacy Timisoara, Romania, 2008
-PCR technique: GeneticLab, Bucharest, Romania, Molecular Department, 2005
-PCR,Southern Blot techniques,DNA sequencing: Molecular Department, Institute of Human Genetics, University of Wuerzburg, Germany, 2004
- Cancer Cytogenetics: Clinical Institute of Pediatrics, Hematology Center, Cytogenetics and Molecular Cytogenetics Department, Debrecen, Hungary, 2002
- FISH, PCR techniques, DNA sequencing: Molecular Cytogenetics and Molecular Laboratories, Institute of Clinical Genetics, Dresden, Germany,2001 and 2002

Other training courses and workshops:
-"26th Course in Medical Genetics", 12-16 May 2013, webcasted from European School of Genetics Medicine, Bologna Italy at the Remote Training Center Al Jawhara Center for Molecular Medicine, Manama Bahrain;
-“Evidenced based medicine “workshop, WHO Collaborating Centre for Educational Development, College of Medicine and Medical Sciences, Arabian Gulf University, 19-20 April 2013, Manama, Bahrain.
- Cochrane Library Seminar, June 2012, Al Jawhara Center, Bahrain
-" Cardiovascular genetics- genetic counselling", Division of Human Genetics, Heart Institute at Cincinnati Children’s Medical Center, online course, May 2012, USA.
-“How to get yourself published in an academic journal”- workshop, RCSI, May 2012,Manama Bahrain
-“2nd Course in Bioinformatics” – Arabian Gulf University, The Biotechnology program, 11-22 March 2012, Manama, Bahrain.
-“Course and program Specifications And Reports”, The Quality Assurance Office and the Saudi National Council for Academic Accreditation and Assessment, Arabian Gulf University, Kingdom of Bahrain,15-16 November 2011
-„Tutoring skills” training program, Arabian Gulf University, College of Medicine and Medical Sciences, Kingdom of Bahrain 15 and 25 January 2011
- "Genetics practical applications in endocrinology- from classical cytogenetics to Molecular genetics techniques”, 19-21May 2010, Tg. Mures, Romania
-„ Project manager”, Ministry of Work, Ministry of Education, Research and Youth,Romania, S.C. Romarketing SRL, April 2010.
- 2nd Course “The integration of cytogenetics, microarrays and massive sequencing in biomedical and clinical research”- 18-22 October 2009, European Genetics Foundation European School of Genetic Medicine, Bologna, Italy.
-„ Project manager”, Ministry of Work, Ministry of Education, Research and Youth,Romania, S.C. Idas Group SRL, June 2009.
- 3rd Course in Clinical Cytogenetics, August 30th- September 4th, Goldrain, South Tirol, Italy.
- „Molecular Cytogenetics techniques using in situ hybridisation”- practical course of molecular cytogenetics, 21-23 May 2008, Timisoara, Romania.
-The 5th German- Romanian Genetics Course, 14-17 April, Oradea, Baile Felix, Romania
-„Actualities in Pediatrics”, Oradea, Romania 7- 11 May 2007
- 7th Course , Genetic Counselling in Practice, Bologna University Residential Center Bertinoro di Romagna, 9-14 November, 2006, Italy.
- The 4th German- Romanian Genetics Course, 21-24 April, Oradea, Romania
- „Actualities in Pediatrics”, Oradea, Romania 3-8 May 2005
Cardiac Morphology 3, 3 December, Gottsegen Hungarian Institute of Cardiology,Pediatric Cardiac, Budapest, Hungary.
- „Actualities in Pediatrics”, Oradea, Romania 26-30 April 2004
- Course „Actualities in Pediatrics”, Oradea, Romania 31 March – 4 april 2003
- The 24th Syndromclub, April 27, Institut of Clinical Genetics, Dresden University of Technology, Germany.
- The 3rd German- Romanian Genetics Course, September 6-7, Oradea,Romania
- The 14th Course in Medical Genetics of European School of Genetic Medicine, March 25-31, La Nunziata Centre, Sestri Levante,Genoa-Italy
- The 10th International Congress of Human Genetics,May 15-19, Vienna
- The 2nd German- Romanian Genetics Course, 6-7 March, Oradea-Arad, Romania

• Professional books- coauthor:
- Coordinator Maria Puiu: „Medical Awarness in rare genetics disorders/ Alerta medicala in bolile genetice rare” ISBN 978-606-8054-39-1 pg.466. Cristina Skrypnyk: pg. 50-81, 268, 384-385,439. Editura Victor Babes, Timisoara, 2011
-Coordinators Mircea Covic, Dragos Stefanescu, Ionel Sandovici: „Medical Genetics- second edition / Genetica Medicala- editia a II-a/”- ISBN 978-973-46-1960-3, pg 713. Chapter 9: Genetics disorders and genomic medicine- authors: M. Covic, G. Tauser, C. Skrypnyk, I. Sandovici, pp.319-344; Chapter 11: Chromosomal disorders- authors: V. Gorduza, C. Popovici, C. Scrypnyk, M. Covic, V. Belengeanu, D. Stoicanescu, M. Panzaru, L. Butnariu, pp.384-416. Editura Polirom Iasi, 2011
-Coordinator Marius Bembea „Izolate genetice din Bihor/ Genetics isolates in Bihor”, ISBN 978-973-759-999-5 pg.181. Colaborators- Kinga Kozma, Claudia Jurca, Cristina Skrypnyk, Serban Bembea, Oana Iuhas, Radu Harbuz, Corina Nagy. Editura Universitatii din Oradea, 2009
-Coordinator Maria Puiu, Cristina Skrypnyk „Mic ghid de diagnostic al bolilor genetice/ Small guide of rare diseases diagnosis”., ISBN 978-606-92022-0-3 pg.183pg. Cristina Skrypnyk: pg. 15-16, 17, 21-22, 73-74, 141-142, 173. Editura Victor Babes, Timisoara, 2009
-Coordinator Cristina Rusu „Metode de screening si diagnostic a bolilor genetice/ Methods for screening and diagnosis of genetics disorders.” Cristina Skrypnyk: pg 113-121, 141-154, 215-223. ISBN 978-973-7682-31-4; 266pg;.Editura Gr. T. Popa U.M.F. Iasi, 2007
-Coordinator Maria Puiu. „Esentialul in 101 boli genetice rare/ Essential in 101 rare genetics disorders”. Cristina Skrypnyk :pg. 66, 67-72, 80-82, 470-472. ISBN 978-973-638-327-4, 511 pg; Editura Orizonturi Universitare, Timisoara, 2007
-Valeria Filip, Cristina Skrypnyk. „ Malformatii de tub neural/ Neural tube defects”. - ISBN (10) 973-87960-1-6, ISBN (13) 978-973-87960- 1-0, 175 pg, Editura Universitatii Agora, Oradea, 2006
-Valeria Filip, Laura Lele, Cristina Skrypnyk „ Nou nascutul la termen/ New born at term”. ISBN (10) 973-87960-0-8, ISBN (13) 978- 973- 87960-0-3, 87 pg Editura Universitatii Agora, Oradea, 2006

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Contact Information

 

Work Tel No: 17237315 Work Fax No: 17246022
cristinas@agu.edu.bh

 

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