Literature DB >> 1063014

The Klippel-Feil syndrome. A rare cause of cervico-facial deformity.

J C Cooper.   

Abstract

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Year:  1976        PMID： 1063014     DOI： 10.1038/sj.bdj.4803748

Source DB:  PubMed          Journal:  Br Dent J        ISSN： 0007-0610            Impact factor:   1.626


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  3 in total

1.  Autosomal recessive Klippel-Feil syndrome.

Authors:  E O Da Silva
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

2.  Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomaly.

Authors:  Jawahir Y Mohamed; Eissa Faqeih; Abdulmonem Alsiddiky; Muneera J Alshammari; Niema A Ibrahim; Fowzan S Alkuraya
Journal:  Am J Hum Genet       Date:  2013-01-03       Impact factor: 11.025

3.  Klippel-Feil syndrome in children: clinical features and management.

Authors:  M G Nagib; R E Maxwell; S N Chou
Journal:  Childs Nerv Syst       Date:  1985       Impact factor: 1.475
  3 in total

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