Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome-Reference-Cited by-同舟云学术

Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome

Published:2003-11-03 Issue:3 Volume:123A Page:236-242
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Johnston Jennifer J.,Olivos-Glander Isabelle,Turner Joyce,Aleck Kyrieckos,Bird Lynne M.,Mehta Lakshmi,Schimke R. Neil,Heilstedt Heidi,Spence J. Edward,Blancato Jan,Biesecker Leslie G.

Publisher

Wiley

Subject

Genetics (clinical)

Reference16 articles.

1. Strike three for GLI3

2. Detection of a subtle rearrangement of chromosome 22 using molecular techniques

3. The acrocallosal syndrome and Greig syndrome are not allelic disorders.

4. The greig cephalopolysyndactyly syndrome in a canadian family

5. Acrocallosal syndrome in Algerian boy born to consanguineous parents: Review of the literature and further delineation of the syndrome

Cited by 50 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. A Rare Prenatal Case: Greig Cephalopolysyndactyly Syndrome;Gazi Medical Journal;2024-04-01

2. Molecular Bases of Human Malformation Syndromes Involving the SHH Pathway: GLIA/R Balance and Cardinal Phenotypes;International Journal of Molecular Sciences;2021-12-02

3. Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review;Genes;2021-10-23

4. PALLISTER–HALL SYNDROME AND GREIG CEPHALOPOLYSYNDACTYLY SYNDROME;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30

5. Variant type and position predict two distinct limb phenotypes in patients with GLI3-mediated polydactyly syndromes;Journal of Medical Genetics;2020-06-26