Cytogenetic analyses on patients with Crouzon's and Apert's syndromes-Reference-Cited by-同舟云学术

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Cytogenetic analyses on patients with Crouzon's and Apert's syndromes

Published:2008-02-14 Issue:1 Volume:105 Page:157-159
ISSN:0018-0661
Container-title:Hereditas
language:en
Short-container-title:

Author:

MARK JOACHIM,LILJA JAN,STENMAN GÖRAN,LAURITZEN CLAES

Publisher

Springer Science and Business Media LLC

Subject

Genetics,General Medicine

Reference7 articles.

1. Terminal 7 p deletion and 1;7 translocation associated with cransynostosis;Dhadial;Hum. Genet.,1979

2. Prenatal phytoscopic diagnosis of the Apert syndrome;Leonard;Am. J. Med. Genet.,1982

3. Interstitial deletion for a region in the long arm of chromosome 16;Lin;Hum. Genet.,1983

4. Chromosome 7 short arm deletion and craniosynostosis. -A 7p syndrome;Mcpherson;Hum. Genet.,1976

5. Loss of the Y chromosome in a cultured human cellular gland adenocarcinoma;Stenman;J. Oral Pathol.,1983

Cited by 3 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. Cytogenetic Survey of Apert Syndrome;American Journal of Diseases of Children;1993-12-01

2. Appendix;Clinics in Plastic Surgery;1991-04

3. Clinical Assessment and Multispecialty Management of Apert Syndrome;Clinics in Plastic Surgery;1991-04

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