Literature DB >> 13613871

Craniofacial dysostosis of Crouzon; a case report and pedigree with emphasis on heredity.

J G SHILLER.   

Abstract

Entities:  

Keywords:  HYPERTELORISM/heredity

Mesh：

Year:  1959        PMID： 13613871

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  7 in total

1.  Cranio-facial Dysostosis in a Dorset Family.

Authors:  D G Vulliamy; P A Normandale
Journal:  Arch Dis Child       Date:  1966-08       Impact factor: 3.791

2.  Studies of malformation syndromes in man XXXVI: the Pfeiffer syndrome, association with Kleeblattschädel and multiple visceral anomalies. Case report and review.

Authors:  R J Hodach; C Viseskul; E F Gilbert; J P Herrmann; J J Wolfson; E G Kaveggia; J M Opitz
Journal:  Z Kinderheilkd       Date:  1975

3.  Germinal mosaicism in Crouzon syndrome.

Authors:  S Kreiborg; M M Cohen
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

4.  Letter: The Crouzon syndrome.

Authors:  K L Jones; M M Cohen
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

5.  An autosomal recessive form of craniofacial dysostosis (the Crouzon syndrome).

Authors:  R C Juberg; S R Chambers
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

6.  Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qter.

Authors:  W Reardon; L van Herwerden; C Rose; B Jones; S Malcolm; R M Winter
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

Review 7.  Revisiting Crouzon syndrome: reviewing the background and management of a multifaceted disease.

Authors:  Samuel N Helman; Arvind Badhey; Sameep Kadakia; Eugene Myers
Journal:  Oral Maxillofac Surg       Date:  2014-09-24
  7 in total

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