Prenatal Diagnosis of Minute Supernumerary Marker Chromosomes-Reference-Cited by-同舟云学术

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Prenatal Diagnosis of Minute Supernumerary Marker Chromosomes

Published:2005 Issue:1 Volume:60 Page:27-38
ISSN:0378-7346
Container-title:Gynecologic and Obstetric Investigation
language:en
Short-container-title:Gynecol Obstet Invest

Author:

Cotter Philip D.,Drexler Kathryn,Corley Amy L.,Covert Susan M.,Moland Jessica S.,Govberg Inna J.,Norton Mary E.

Publisher

S. Karger AG

Subject

Obstetrics and Gynecology,Reproductive Medicine

Reference47 articles.

1. ISCN: An International System for Human Cytogenetic Nomenclature. Basel, Karger, 1995.

2. Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescencein situ hybridization

3. Forty four probands with an additional ?marker? chromosome

4. Delineation of supernumerary marker chromosomes in 38 patients

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1. Retrospectively investigating the 12-year experience of prenatal diagnosis of small supernumerary marker chromosomes through array comparative genomic hybridization;Taiwanese Journal of Obstetrics and Gynecology;2019-01

2. Socioeconomic differentials in mortality by cause of death in the Republic of Ireland, 1984–2008;The European Journal of Public Health;2016-04-11

3. Mosaic small supernumerary marker chromosome 1 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review;Gene;2013-10

4. Reestructuraciones compatibles con un fenotipo normal detectadas en diagnóstico prenatal;Diagnóstico Prenatal;2013-07

5. Molecular characterization of 39 de novo sSMC : contribution to prognosis and genetic counselling, a prospective study;Clinical Genetics;2013-04-05

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