Partial trisomy 11q due to paternal t(11q;18p); further delineation of the clinical picture-Reference-Cited by-同舟云学术

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Partial trisomy 11q due to paternal t(11q;18p); further delineation of the clinical picture

Published:2008-04-23 Issue:3 Volume:25 Page:295-299
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

France H. F. de,Beemer F. A.,Senders R. Ch.,Gerards L. J.,Cats B. P.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1984.tb01992.x/fullpdf

Reference3 articles.

1. Das 18p- Syndrom;Aksu;Mschr. Kinderheilk,1977

2. The 11q;22q Translocation: an European Collaborative Analysis of 43 cases;Fraccaro;Hum. Genet,1980

3. Partial 11q Trisomy Syndrome;Pihko;Hum. Genet,1981

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical and molecular evaluations of siblings with “pure” 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3);Molecular Cytogenetics;2014-12

2. Identification of genomic loci contributing to agenesis of the corpus callosum;American Journal of Medical Genetics Part A;2010-08-03

3. Monosomy 10q26-qter and trisomy 11q13-qter as a result ofde novo unbalanced translocation;Journal of Applied Genetics;2009-09

4. Congenital cardiovascular malformations (CCVM) and structural chromosome abnormalities: a report of 9 cases and literature review;Clinical Genetics;2008-06-28

5. De novo 46,XX, dir dup (11)(q13.3→q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopenia;Clinical Genetics;2008-06-28

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