Craniofrontonasal dysostosis: variable expression in a three-generation family
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1990.tb03610.x/fullpdf
Reference21 articles.
1. Chromosomal localization of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13;Brueton;Am. J. Med. Genet.,1988
2. Craniofrontonasal dysplasia;Cohen;Birth Defects: Original Article Series,1979
3. Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly;Hunter;Teratology,1977
4. A family with craniofrontonasal dysplasia and fragile site 12q13 segregating independently;Kumar;Clin. Genet.,1986
5. Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression;Kwee;Clin. Genet.,1983
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