Literature DB >> 12491086

Disruption of the C7orf2/Lmbr1 genic region is associated with preaxial polydactyly in humans and mice.

Taizo Horikoshi1, Naoto Endo, Minoru Shibata, Peter Heutink, Robert E Hill, Sumihare Noji.   

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Year:  2003        PMID： 12491086     DOI： 10.1007/s007740300000

Source DB:  PubMed          Journal:  J Bone Miner Metab        ISSN： 0914-8779            Impact factor:   2.626


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  3 in total

Review 1.  Genetic disorders of the skeleton: a developmental approach.

Authors:  Uwe Kornak; Stefan Mundlos
Journal:  Am J Hum Genet       Date:  2003-07-31       Impact factor: 11.025

2.  Identification of an alternative splicing isoform of chicken Lmbr1.

Authors:  Yanqun Huang; Wen Chen; Ning Li; Xuemei Deng; Xiangtao Kang; Xiaojun Liu
Journal:  Mol Biol Rep       Date:  2010-12-15       Impact factor: 2.316

3.  Canine polydactyl mutations with heterogeneous origin in the conserved intronic sequence of LMBR1.

Authors:  Kiyun Park; Joohyun Kang; Krishna Pd Subedi; Ji-Hong Ha; Chankyu Park
Journal:  Genetics       Date:  2008-08-09       Impact factor: 4.562
  3 in total

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