Further evidence from two families that craniofrontonasal dysplasia maps to Xp22

Author:

Pulleyn Lj,Winter Rm,Reardon W,McKeown C,Jones B,Hayward R,Evans R,Malcolm S

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference14 articles.

1. Craniofrontonasal dysplasia;Cohen;Birth Defects,1979

2. Craniofrontonasal dysplasia;Kapusta;Eur J Pediatr,1992

3. Craniofrontonasal dysostosis: variable expression in a three-generation family;Kere;Clin Genet,1990

4. Craniofrontonasal dysplasia (CFND): continuing evidence for Johnson's metabolic interference hypothesis for an X-linked locus;Smith;Am J Hum Genet,1990

5. Craniofrontonasal dysplasia: phenotypic expression in females and males and genetic considerations;Grutzner;Oral Surg Oral Med Oral Pathol,1988

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

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