Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing-Reference-Cited by-同舟云学术

Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing

Published:2015-04 Issue:4 Volume:45 Page:394-401
ISSN:0960-7692
Container-title:Ultrasound in Obstetrics & Gynecology
language:en
Short-container-title:Ultrasound Obstet Gynecol

Author:

Cohen K.¹²,Tzika A.³,Wood H.²,Berri S.²⁴,Roberts P.³,Mason G.¹,Sheridan E.²

Affiliation:

1. Department of Fetal Medicine; Leeds General Infirmary; Leeds UK

2. Leeds Institute of Cancer and Pathology; Leeds UK

3. Department of Cytogenetics; St James's University Hospital; Leeds UK

4. Illumina UK Ltd; Chesterford Research Park, Little Chesterford Essex UK

Funder

Wellbeing of Women

Publisher

Wiley

Subject

Obstetrics and Gynaecology,Radiology Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Reference15 articles.

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4. Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH;Bi;Prenat Diagn,2008

5. Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis;Hehir-Kwa;DNA Res,2007

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