Clinical features in a de novo interstitial deletion 15q13 to q15
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1988.tb02881.x/fullpdf
Reference10 articles.
1. Adjacent 2 meiotic disjunction. Report of a case resulting from a familial 13q;15q balanced reciprocical translocation and review of the literature;Duckett;Hum. Genet.,1981
2. Interstitial deletion of the long arm of chromosome 15;Fryns;Ann. Genet. (Paris),1982
3. Congenital heart disease with del (15q) mosaicism;Herva;Clin. Genet.,1980
4. Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high resolution chromosome banding;Ikeuchi;Cytogenet. Cell Genet.,1984
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1. Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot;Taiwanese Journal of Obstetrics and Gynecology;2016-04
2. Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndrome;Orphanet Journal of Rare Diseases;2011
3. Identification of genomic loci contributing to agenesis of the corpus callosum;American Journal of Medical Genetics Part A;2010-08-03
4. An interstitial 15q11-q14 deletion: Expanded Prader-Willi syndrome phenotype;American Journal of Medical Genetics Part A;2010-02
5. Molecular and clinical characterization of two patients with Prader-Willi syndrome and atypical deletions of proximal chromosome 15q;American Journal of Medical Genetics Part A;2008-08-01
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