The use of chromosomal microarray in prenatal diagnosis-Reference-Cited by-同舟云学术

The use of chromosomal microarray in prenatal diagnosis

Published:2013-04 Issue:2 Volume:15 Page:80-84
ISSN:1467-2561
Container-title:The Obstetrician & Gynaecologist
language:en
Short-container-title:Obstet Gynecol

Author:

Hillman Sarah¹,McMullan Dominic J²,Maher Eamonn R,Kilby Mark D

Affiliation:

1. School of Clinical and Experimental Medicine; College of Medicine and Dentistry; University of Birmingham; Edgbaston; Birmingham; B15 2TT; UK

2. West Midlands Regional Genetics Laboratories and the Department of Clinical Genetics; Birmingham Women's Foundation Trust; Edgbaston; Birmingham; B15 2TG; UK

Publisher

Wiley

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/tog.12007/fullpdf

Reference22 articles.

1. Chromosome analysis of human amniotic-fluid cells;Steele;Lancet,1966

2. Prental detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18 and 21 FISH or PCR without a full karyotype: a cytogenetic risk assessment;Aine;Lancet,2005

3. Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies;Langlois;J Obstet Gynaecol Can,2011

4. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies;Miller;Am J Hum Genet,2010

5. Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy;Bodrug;J Med Genet,1990

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