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Mosaic trisomy 16 ascertained through amniocentesis : Evaluation of 11 new cases

Author
HSU, W.-T1 ; SHCHEPIN, D. A1 ; HAJIANPOUR, M. J5 ; WANG, J.-C. C5 ; ROSENBLUM-VOS, L. S6 ; BHATT, S. D7 ; KARSON, E. M8 ; HUX, C. H9 ; TRUNCA, C10 ; BIALER, M. G11 ; LINN, S. K12 ; SCHRECK, R. R2 ; RONG MAO1 ; BERRY-KRAVIS, E1 ; GARBER, A. P2 ; FISCHEL-GHODSIAN, N2 ; FALK, R. E2 ; CARLSON, D. E2 ; ROEDER, E. R3 ; LEETH, E. A4
[1] Department of Pediatrics, Rush Medical College, Chicago, Illinois, United States
[2] Medical Genetics Birth Defects Center, Cedars Sinai Medical Center, UCLA School of Medicine, Los Angeles, California, United States
[3] Genetic Medicine, Valley Children Hospital, Fresno, California, United States
[4] Obstetrics & Gynecology, Evanston Hospital, Evanston, Illinois, United States
[5] The Genetics Institute, Pasadena, California, United States
[6] Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States
[7] Genzyme Genetics, Orange, California, United States
[8] Columbia Hospital for Women Medical Center, Washington, D.C, United States
[9] Department of Obstetrics & Gynecology, Jersey Shore Medical Center, Neptune, New Jersey, United States
[10] The Genetics Center, Inc., Smithtown, New York, United States
[11] Division of Child Development and Human Genetics, North Shore University Hospital, Manhasset, New York, United States
[12] Reproductive Genetics Center, Denver, Colorado, United States
Source

American journal of medical genetics. = Neuropsychiatric genetics. 1998, Vol 80, Num 5, pp 473-480 ; ref : 1 p.1/4

CODEN
AJMGDA
ISSN
0148-7299
Scientific domain
Genetics
Publisher
Wiley-Liss, New York, NY
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Amniocentèse Chromosome E16 Deuxième trimestre Diagnostic Disomie uniparentale Homme Mosaïcisme Phénotype Pronostic Prénatal Trisomie Aberration chromosomique Aneuploïdie Génétique
Keyword (en)
Amniocentesis Chromosome E16 Second trimester Diagnosis Uniparental disomy Human Mosaicism Phenotype Prognosis Prenatal Trisomy Chromosomal aberration Aneuploidy Genetics
Keyword (es)
Amniocentesis Cromosoma E16 Segundo trimestre Diagnóstico Disomia uniparental Hombre Mosaicismo Fenotipo Pronóstico Prenatal Trisomía Aberración cromosómica Aneuploidía Genética
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
1610791

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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