Unexpected detection of dystrophin gene deletions by array comparative genomic hybridization-Reference-Cited by-同舟云学术

Unexpected detection of dystrophin gene deletions by array comparative genomic hybridization

Published:2010-08-03 Issue:9 Volume:152A Page:2301-2307
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Cottrell Catherine E.,Prior Thomas W.,Pyatt Robert,Astbury Caroline,Reshmi Shalini,Bartholomew Dennis,Atkin Joan,Manickam Kandamurugu,Thrush Devon Lamb,Pastore Matthew,Mendell Jerry,Tsao Chang-Yong,al-Dahhak Roula,Newmeyer Amy,Gastier-Foster Julie M.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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4. Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy;Beroud;Hum Mutat,2007

5. Frequency of new mutants among boys with Duchenne muscular dystrophy;Bucher;Am J Med Genet,1980

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2. Incidental prenatal detection of DMD gene deletion using array comparative genomic hybridization;European Journal of Obstetrics & Gynecology and Reproductive Biology;2016-08

3. Clinical experience of unexpected findings in prenatal array testing;Biomarkers in Medicine;2016-08

4. Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs;European Journal of Human Genetics;2015-09-02

5. Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family history;Clinical Genetics;2014-07-21