Phenotypic overlapping of trisomy 12p and Pallister–Killian syndrome-Reference-Cited by-同舟云学术

Phenotypic overlapping of trisomy 12p and Pallister–Killian syndrome

Published:2010-05 Issue:3 Volume:53 Page:159-161
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Inage Eisuke,Suzuki Mitsuyoshi,Minowa Kei,Akimoto Nahoko,Hisata Ken,Shoji Hiromichi,Okumura Akihisa,Shimojima Keiko,Shimizu Toshiaki,Yamamoto Toshiyuki

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference11 articles.

1. Cytogenetic and molecular analysis in trisomy 12p;Allen;Am. J. Med. Genet.,1996

2. Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation;Liehr;Cytogenet. Genome Res.,2006

3. Clinical and molecular cytogenetic observations in three cases of “trisomy 12p syndrome”;Rauch;Am. J. Med. Genet.,1996

4. The natural history of trisomy 12p;Segel;Am. J. Med. Genet. A,2006

5. A familial 593-kb microdeletion of 16p11.2 associated with mental retardation and hemivertebrae;Shimojima;Eur. J. Med. Genet.,2009

Cited by 16 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. Skin and Lacrimal Drainage System;Ocular Pathology;2025

2. Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children;Orphanet Journal of Rare Diseases;2024-03-08

3. Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases;The Journal of Pediatrics;2022-07

4. Prenatal diagnosis of the Dandy–Walker malformation associated with partial trisomy 12p and distal 15q deletion;Journal of Genetics;2021-06-02

5. Pallister–Killian Syndrome versus Trisomy 12p—A Clinical Study of 5 New Cases and a Literature Review;Genes;2021-05-26