Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: Phenotypic and genotypic findings-Reference-Cited by-同舟云学术

Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: Phenotypic and genotypic findings

Published:2013-03 Issue:1 Volume:517 Page:137-145
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Shojaei Azadeh,Behjati Farkhondeh,Derakhshandeh-Peykar Pupak,Razzaghy-Azar Maryam,Otukesh Hasan,Kariminejad Roxana,Dowlati Mohammad-Ali,Rashidi-Nezhad Ali,Tavakkoly-Bazzaz Javad

Funder

Tehran University of Medical Sciences (TUMS)

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference27 articles.

1. Is Dandy–Walker malformation associated with “distal 13q deletion syndrome”? Findings in a fetus supporting previous observations;Alanay;Am. J. Med. Genet. A,2005

2. A new case of pure partial 7q duplication;Alfonsi;Cytogenet. Genome Res.,2012

3. 13q Deletion and central nervous system anomalies: further insights from karyotype–phenotype analyses of 14 patients;Ballarati;J. Med. Genet.,2007

4. Partial monosomy 13q and partial trisomy 18p: case report with necropsy findings;Beneck;J. Med. Genet.,1986

5. Preliminary definition of a “critical region” of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature;Brown;Am. J. Med. Genet.,1993

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