Molecular exclusion of Haemoglobin SD disease by prenatal diagnosis
- Author
- FODOR, F. H1 ; ENG, C. M1
[1] Department of Human Genetics, Mount Sinai School of Medicine, New York, United States - Source
Prenatal diagnosis. 1999, Vol 19, Num 1, pp 58-60 ; ref : 8 ref
- CODEN
- PRDIDM
- ISSN
- 0197-3851
- Scientific domain
- Genetics; Obstetrics, gynecology, andrology; General medicine general surgery; Neonatology
- Publisher
- Wiley, Chichester
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Biologie moléculaire DNA Diagnostic Etude cas Foetus Hémoglobine D Hémoglobinopathie Prénatal Technique Anémie hémolytique Hémopathie
- Keyword (en)
- Molecular biology DNA Diagnosis Case study Fetus Hemoglobin D Hemoglobinopathy Prenatal Technique Hemolytic anemia Hemopathy
- Keyword (es)
- Biología molecular DNA Diagnóstico Estudio caso Feto Hemoglobina D Hemoglobinopatía Prenatal Técnica Anemia hemolítica Hemopatía
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B20 Gynecology. Andrology. Obstetrics / 002B20F Pregnancy. Fetus. Placenta / 002B20F01 Management. Prenatal diagnosis
- Discipline
- Gynecology. Andrology. Obstetrics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 1673564
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1002/(SICI)1097-0223(199901)19:1<58::AID-PD453>3.0.CO;2-1 
https://dx.doi.org/10.1002/(SICI)1097-0223(199901)19:1<58::AID-PD453>3.0.CO;2-1
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