The Greig polysyndactyly craniofacial dysmorphism syndrome: Variable expression in a family
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF00441928.pdf
Reference5 articles.
1. Fryns JP, Coeck W, Van Den Berghe H (1977) The Greig polysyndactyly-craniofacial dysmorphism syndrome. Europ J Pediatr 126:283?287
2. Greig DM (1926) Oxycephaly. Edinb Med J 33:189?218
3. Hootnick D, Holmes LB (1972) Familial polysyndactyly and craniofacial anomalies. Clin Genet 3:128?134
4. Marshall RE, Smith DW (1970) Frontodigital syndrome: a dominantly inherited disorder with normal intelligence. J Pediatr 77:129?133
5. Temtamy S, McKusick VA (1969) Synopsis on hand malformations with particular emphasis on genetic factors. Birth Defects (Series V) 3:125?184
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1. Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3;European Journal of Human Genetics;2011-02-16
2. Greig cephalopolysyndactyly: report of 13 affected individuals in three families;Clinical Genetics;2008-04-23
3. The spectrum of hand and foot malformations in patients with Greig cephalopolysyndactyly;Journal of Children's Orthopaedics;2007-07-01
4. Japanese family with Greig cephalopolysyndactyly syndrome, including bilateral seven toes, and esotropia, over three generations;Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery;2006-01
5. Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identifiedGLI3 mutations;American Journal of Medical Genetics;2003-06-03
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