Expanding the phenotype of feingold syndrome-2-Reference-Cited by-同舟云学术

Expanding the phenotype of feingold syndrome-2

Published:2015-09-11 Issue:12 Volume:167 Page:3219-3225
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Grote Lauren E.¹,Repnikova Elena A.²,Amudhavalli Shivarajan M.¹

Affiliation:

1. Division of Clinical Genetics; Children's Mercy Hospital; University of Missouri-Kansas City School of Medicine; Kansas City Missouri

2. Cytogenetics and Molecular Genetics Laboratories; Children's Mercy Hospital; University of Missouri-Kansas City School of Medicine; Kansas City Missouri

Funder

Wellcome Trust

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference16 articles.

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3. Feingold syndrome: Clinical review and genetic mapping;Celli;Am J Med Genet Part A,2003

4. A high resolution in situ hybridization technique for the direct visualization of labeled G-banded early metaphase and prophase chromosomes;Chandler;Cytogenetics and Cell Genetics,1978

5. Germline deletion of the miR-17-92 cluster causes skeletal and growth defects in humans;De Pontual;Nat Genet,2011

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