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Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited marker

Author
KULHARYA, A. S1 ; GARCIA-HERAS, J2 ; RADTKE, H. B1 ; NORRIS, K. S1 ; KEPPEN, L. D3 ; FLANNERY, D. B1
[1] Department of Pediatrics, Medical College of Georgia, Augusta, GA, United States
[2] Genetic Testing Center, Bureau of Laboratories, Texas Department of Health, Denton, TX, United States
[3] Department of Pediatrics, University of South Dakota School of Medicine, Sioux Falls, SD, United States
Source

Clinical genetics. 1998, Vol 54, Num 5, pp 421-425 ; ref : 17 ref

CODEN
CLGNAY
ISSN
0009-9163
Scientific domain
Genetics
Publisher
Blackwell, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Bras court Chromosome E17 anormal Chromosome surnuméraire DNA satellite De novo Diagnostic Nourrisson Phénotype Prénatal Trisomie partielle Aberration chromosomique Aneuploïdie Chromosome anormal Homme
Keyword (en)
Short arm Abnormal chromosome E17 Supernumerary chromosome Satellite DNA De novo Diagnosis Infant Phenotype Prenatal Partial trisomy Chromosomal aberration Aneuploidy Abnormal chromosome Human
Keyword (es)
Brazo corto Cromosoma E17 anormal Cromosoma supernumerario DNA satélite De novo Diagnóstico Lactante Fenotipo Prenatal Trisomía parcial Aberración cromosómica Aneuploidía Cromosoma anormal Hombre
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23B Chromosome aberrations

Discipline
Medical genetics
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
1657477

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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