Use of single nucleotide polymorphism microarrays to distinguish between balanced and normal chromosomes in embryos from a translocation carrier-Reference-Cited by-同舟云学术

Use of single nucleotide polymorphism microarrays to distinguish between balanced and normal chromosomes in embryos from a translocation carrier

Published:2011-07 Issue:1 Volume:96 Page:e58-e65
ISSN:0015-0282
Container-title:Fertility and Sterility
language:en
Short-container-title:Fertility and Sterility

Author:

Treff Nathan R.,Tao Xin,Schillings Wendy J.,Bergh Paul A.,Scott Richard T.,Levy Brynn

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,Reproductive Medicine

Reference19 articles.

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2. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation;Simovich;Prenat Diagn,2007

3. Detection of an interstitial deletion of 2q21–22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocation;Shanske;Am J Med Genet,2004

4. Detection of deletions in de novo “balance” chromosome rearrangements: further evidence for their role in phenotypic abnormalities;Astbury;Gene Med,2004

5. High resolution comparative genomic hybridization in clinical cytogenetics;Kirchhoff;J Med Genet,2001

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