Germinal mosaicism in Crouzon syndrome-Reference-Cited by-同舟云学术

Germinal mosaicism in Crouzon syndrome

Published:1990-04 Issue:5 Volume:84 Page:487-488
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Kreiborg Sven,Cohen M. Michael

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00195827.pdf

Reference14 articles.

1. Allanson JE (1986) Germinal mosaicism in Apert syndrome. Clin Genet 29:429–433

2. Cohen MM Jr (1986) Syndromes with craniosynostosis. In: Cohen MM Jr (ed) Craniosynostosis: diagnosis, evaluation, and management. Raven Press, New York, pp 413–590

3. Cross HE, Opitz JM (1969) Craniosynostosis in the Amish. J Pediatr 75:1037–1044

4. Fogh-Andersen P (1943) Craniofacial dysostosis (Crouzon) as a dominantly inherited disease (in Danish). Nord Med 18:993–996

5. Fryns JP, Kleczkowski A, Verresen H, Berghe H van den (1983) Germinal mosaicism in achondroplasia. A family with 3 affected siblings of normal parents. Clin Genet 24:156–158

Cited by 11 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. Genetics of Craniosynostosis;Youmans Neurological Surgery;2011

2. Germline and somatic mosaicism for FGFR2 mutation in the mother of a child with Crouzon syndrome: Implications for genetic testing in “paternal age-effect” syndromes;American Journal of Medical Genetics Part A;2010-07-15

3. A Novel FGFR2 Gene Mutation in Crouzon Syndrome Associated with Apparent Nonpenetrance;The Cleft Palate-Craniofacial Journal;1999-11

4. Cephalometric analysis of families with dominantly inherited Crouzon syndrome: An aid to diagnosis in family studies;American Journal of Medical Genetics;1998-06-05

5. Dentofacial features of a family with Crouzon syndrome. Case reports;Australian Dental Journal;1997-02