Prenatal diagnosis for thalassaemia in Egypt: what changed parents' attitude?-Reference-Cited by-同舟云学术

Prenatal diagnosis for thalassaemia in Egypt: what changed parents' attitude?

Published:2012-06-13 Issue:8 Volume:32 Page:777-782
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

El-Beshlawy A.¹,El-Shekha A.²,Momtaz M.²,Said F.³,Hamdy M.¹,Osman O.²,Meshaal S.³,Gafaar T.³,Petrou M.⁴

Affiliation:

1. Pediatric Hematology Department; Cairo University; Cairo; Egypt

2. Fetal Medicine Department; Cairo University; Cairo; Egypt

3. Clinical Pathology Department; Cairo University; Cairo; Egypt

4. Institute of Women's Health and Centre for Health Informatics and Multiprofessional Education (CHIME) and University College London Hospitals NHS Foundation Trust Pathology Division; University College London; UK

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference36 articles.

1. Screening for β-thalassemia carriers in Egypt: Significance of the osmotic fragility test;El-Beshlawy;East Mediterr Health J,2007

2. Molecular characterization of β thalassemia mutations in Egypt;Novelletto;Hum Genet,1990

3. Prenatal diagnosis of thalassemia and Hb S syndromes in Greece: an evaluation of 1500 cases;Loukopoulos;Ann NY Acad Sci,1985

4. Current status of thalassaemia and the sickle cell syndromes in Greece;Loukopoulos;Seminars Hematol,1996

5. How thalassaemia was controlled in Cyprus;Angastiniotis;World Health Forum,1986

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