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Prenatal detection of two different monosomic cell lines by chorionic villus sampling

Author
HSU, T.-Y1 ; LIOU, J.-D1 ; COPEL, J. A; MAHONEY, M. J1 ; BREG, W. R1 ; YANG-FENG, T. L1
[1] Yale univ. school medicine, dep. genetics, New Haven CT 06510, United States
Source

Prenatal diagnosis. 1996, Vol 16, Num 2, pp 169-172 ; ref : 16 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)
Aberration chromosomique Caryotype Chromosome G21 Chromosome X Cytogénétique Diagnostic Homme Monosomie Mosaïcisme Prélèvement Prénatal Villosité choriale Aneuploïdie
Keyword (en)
Chromosomal aberration Karyotype Chromosome G21 X-Chromosome Cytogenetics Diagnosis Human Monosomy Mosaicism Samplings Prenatal Chorionic villi Aneuploidy
Keyword (es)
Aberración cromosómica Cariotipo Cromosoma G21 Cromosoma X Citogenética Diagnóstico Hombre Monosomía Mosaicismo Toma de muestra Prenatal Vellosidad coriónica Aneuploidía
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B20 Gynecology. Andrology. Obstetrics / 002B20F Pregnancy. Fetus. Placenta / 002B20F02 Diseases of mother, fetus and pregnancy

Discipline
Gynecology. Andrology. Obstetrics
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
3024997

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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