Literature DB >> 21358539

A clinical report and further delineation of the 14q32 deletion syndrome.

Erin L Youngs1, Jessica A Hellings, Merlin G Butler.   

Abstract

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Year:  2011        PMID： 21358539     DOI： 10.1097/MCD.0b013e3283438200

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  4 in total

1.  14q32 deletion syndrome: a clinical report.

Authors:  Erin L Youngs; Majed Dasouki; Merlin G Butler
Journal:  Clin Dysmorphol       Date:  2012-01       Impact factor: 0.816

2.  Dysregulation of FOXG1 by ring chromosome 14.

Authors:  Daniela Alosi; Laura Line Klitten; Mads Bak; Helle Hjalgrim; Rikke Steensbjerre Møller; Niels Tommerup
Journal:  Mol Cytogenet       Date:  2015-04-09       Impact factor: 2.009

3.  Prenatal diagnosis of a fetus with congenital heart defect and ring chromosome 14.

Authors:  Javier Sánchez; Lutgardo García-Díaz; David Chinchón; Guillermo Antiñolo
Journal:  Case Rep Genet       Date:  2012-11-05

4.  Chromosome deletion of 14q32.33 detected by array comparative genomic hybridization in a patient with features of dubowitz syndrome.

Authors:  Diana C Darcy; Scott Rosenthal; Robert J Wallerstein
Journal:  Case Rep Genet       Date:  2011-09-28
  4 in total

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