Microarray testing in clinical diagnosis: an analysis of 5,300 New Zealand patients-Reference-Cited by-同舟云学术

Microarray testing in clinical diagnosis: an analysis of 5,300 New Zealand patients

Published:2016-03-31 Issue:1 Volume:9 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Mc Cormack Adrian,Claxton Karen,Ashton Fern,Asquith Philip,Atack Edward,Mazzaschi Roberto,Moverley Paula,O’Connor Rachel,Qorri Methat,Sheath Karen,Love Donald R.,George Alice M.

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry (medical),Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-016-0237-9

Reference22 articles.

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3. Ahn JW, Bint S, Bergbaum A, Mann K, Hall RP, Ogilvie CM. Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years’ clinical application for over 8,700 patients. Mol Cytogenet. 2013;6(1):16.

4. Willemsen MH, de Leeuw N, de Brouwer AP, Pfundt R, Hehir-Kwa JY, Yntema HG, et al. Interpretation of clinical relevance of X-chromosome copy number variations identified in a large cohort of individuals with cognitive disorders and/or congenital anomalies. Eur J Med Genet. 2012;55(11):586–98.

5. Coutton C, Dieterich K, Satre V, Vieville G, Amblard F, David M, et al. Array-CGH in children with mild intellectual disability: a population-based study. Eur J Pediatr. 2015;174(1):75–83.

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