Postaxial polydactyly as heterozygote manifestation in Ellis-Van Creveld syndrome?-Reference-Cited by-同舟云学术

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Postaxial polydactyly as heterozygote manifestation in Ellis-Van Creveld syndrome?

Published:1991-06-15 Issue:4 Volume:39 Page:500-500
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Fryns Jean-Pierre

Publisher

Wiley

Subject

Genetics (clinical)

Reference3 articles.

1. Obesity, hypertension, and renal disease in relatives of Bardet-Biedl syndrome sibs

2. A genetic-diagnostic survey in an institutionalized population of 173 severely mentally retarded patients

3. Clinical consequences of heterozygosity for autosomal-recessive diseases*,**

Cited by 13 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. Familial thrombocytosis caused by the novel germ-line mutation p.Pro106Leu in theMPLgene;British Journal of Haematology;2009-01

2. Symptomatic heterozygosity in the Ellis-van Creveld syndrome?;Clinical Genetics;2008-04-23

3. THE FETAL MUSCULOSKELETAL SYSTEM;Ultrasonography in Obstetrics and Gynecology;2008

4. Ellis-Van Creveld syndrome;Orphanet Journal of Rare Diseases;2007-06-04

5. C;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

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