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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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