Literature DB >> 4469994

Symphalangism and brachydactyly syndrome: report of the WL symphalangism-brachydactyly syndrome: review of literature and classification.

J Herrmann.   

Abstract

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Year:  1974        PMID： 4469994

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  6 in total

1.  Classification and identification of inherited brachydactylies.

Authors:  N Fitch
Journal:  J Med Genet       Date:  1979-02       Impact factor: 6.318

2.  Brachydactyly, distal symphalangism, scoliosis, tall stature, and club feet: a new syndrome.

Authors:  D O Sillence
Journal:  J Med Genet       Date:  1978-06       Impact factor: 6.318

3.  A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN.

Authors:  K Lehmann; P Seemann; F Silan; T O Goecke; S Irgang; K W Kjaer; S Kjaergaard; M J Mahoney; S Morlot; C Reissner; B Kerr; A O M Wilkie; S Mundlos
Journal:  Am J Hum Genet       Date:  2007-06-08       Impact factor: 11.025

4.  Multiple synostosis syndrome.

Authors:  J C Pedersen; J P Fryns; G Carpentier; G Heremans; H Van den Berghe
Journal:  Eur J Pediatr       Date:  1980-09       Impact factor: 3.183

5.  Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.

Authors:  Xiao-Lin Wu; Ming-Min Gu; Lei Huang; Xue-Song Liu; Hong-Xin Zhang; Xiao-Yi Ding; Jian-Qiang Xu; Bin Cui; Long Wang; Shun-Yuan Lu; Xiao-Yi Chen; Hai-Guo Zhang; Wei Huang; Wen-Tao Yuan; Jiang-Ming Yang; Qun Gu; Jian Fei; Zhu Chen; Zhi-Min Yuan; Zhu-Gang Wang
Journal:  Am J Hum Genet       Date:  2009-07       Impact factor: 11.025

6.  Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22.

Authors:  D Krakow; K Reinker; B Powell; R Cantor; M A Priore; A Garber; R S Lachman; D L Rimoin; D H Cohn
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025
  6 in total

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