Literature DB >> 201464

The Greig polysyndactyly-craniofacial dysmorphism syndrome.

J P Fryns, W Coeck, H van den Berghe.   

Abstract

A 15-month-old male child with the Greig polysyndactyly-craniofacial dysmorphism syndrome is presented and the relevant literature is reviewed.

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Mesh：

Year:  1977        PMID： 201464     DOI： 10.1007/bf00477055

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


  4 in total

1.  Acrocephalopolysyndactyly, type Noack, in a large kindred.

Authors:  M Robinow; T J Sorauf
Journal:  Birth Defects Orig Artic Ser       Date:  1975

2.  Familial polysyndactyly and craniofacial anomalies.

Authors:  D Hootnick; L B Holmes
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

3.  Frontodigital syndrome: a dominantly inherited disorder with normal intelligence.

Authors:  R E Marshall; D W Smith
Journal:  J Pediatr       Date:  1970-07       Impact factor: 4.406

4.  Carpenter's syndrome: acrocephalopolysyndactyly. An autosomal recessive syndrome.

Authors:  S A Temtamy
Journal:  J Pediatr       Date:  1966-07       Impact factor: 4.406
  4 in total
  3 in total

1.  Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.

Authors:  A L Pettigrew; F Greenberg; C T Caskey; D H Ledbetter
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

2.  The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family.

Authors:  J P Fryns; G Van Noyen; H Van den Berghe
Journal:  Eur J Pediatr       Date:  1981-05       Impact factor: 3.183

3.  The spectrum of hand and foot malformations in patients with Greig cephalopolysyndactyly.

Authors:  Philippe Debeer; Koen Devriendt; Luc De Smet; Thomy Deravel; Antonio Gonzalez-Meneses; Karl-Heinz Grzeschik; Jean-Pierre Fryns
Journal:  J Child Orthop       Date:  2007-05-10       Impact factor: 1.548
  3 in total

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