Two Craniosynostotic Syndrome Loci, Crouzon and Jackson-Weiss, Map to Chromosome 10q23-q26-Reference-Cited by-同舟云学术

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Two Craniosynostotic Syndrome Loci, Crouzon and Jackson-Weiss, Map to Chromosome 10q23-q26

Published:1994-07 Issue:2 Volume:22 Page:418-424
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Li Xiang,Lewanda Amy Feldman,Eluma Fabian,Jerald Heather,Choi Hoon,Alozie Ihuoma,Proukakis Christos,Talbot C.Conover,Kolk Craig Vander,Bird Lynne M.,Jones Marilyn C.,Cunningham Michael,Clarren Sterling K.,Pyeritz Reed E.,Weissenbach Jean,Jackson Charles E.,Jabs Ethylin Wang

Publisher

Elsevier BV

Subject

Genetics

Cited by 32 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. Structural Genome Variations Related to Craniosynostosis;Molecular Syndromology;2018-07-07

2. Craniosynostosis: current conceptions and misconceptions;AIMS Genetics;2016-05

3. Peptide Lv augments L-type voltage-gated calcium channels through vascular endothelial growth factor receptor 2 (VEGFR2) signaling;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2015-05

4. Hearing loss in syndromic craniosynostoses: Otologic manifestations and clinical findings;International Journal of Pediatric Otorhinolaryngology;2014-12

5. Talocalcaneal coalition in Muenke syndrome: Report of a patient, review of the literature in FGFR-related craniosynostoses, and consideration of mechanism;American Journal of Medical Genetics Part A;2013-02-01

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