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Prenatal diagnosis and genetic analysis of double trisomy 48,XXX, +18

Author
CHEN, Chih-Ping1 2 ; CHERN, Schu-Rern2 ; YEH, Li-Fan1 ; CHEN, Wen-Lin1 ; CHEN, Li-Feng1 ; WANG, Wayseen2
[1] Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan, Province of China
[2] Department of Medical Research, Mackay Memorial Hospital and National Yang-Ming University, Taipei, Taiwan, Province of China
Source

Prenatal diagnosis. 2000, Vol 20, Num 9, pp 750-753 ; ref : 25 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)
Association Caryotype Chromosome E18 Chromosome X Diagnostic Déterminisme génétique Etude cas Foetus Homme Prénatal Trisomie Aberration chromosomique Aneuploïdie Cytogénétique
Keyword (en)
Association Karyotype Chromosome E18 X-Chromosome Diagnosis Genetic determinism Case study Fetus Human Prenatal Trisomy Chromosomal aberration Aneuploidy Cytogenetics
Keyword (es)
Asociación Cariotipo Cromosoma E18 Cromosoma X Diagnóstico Determinismo genético Estudio caso Feto Hombre Prenatal Trisomía Aberración cromosómica Aneuploidía Citogenética
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
1497879

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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