Literature DB >> 4659166

Further data on acheiropody.

S P Toledo, P H Saldanha, A Borelli, A B Cintra.   

Abstract

Mesh：

Year:  1972        PMID： 4659166

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


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  3 in total

1.  Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene.

Authors:  P Ianakiev; M J Daly; S P Toledo; M G Cavalcanti; J C Neto; E L Silveira; A Freire-Maia; P Heutink; M W Kilpatrick; P Tsipouras
Journal:  Am J Hum Genet       Date:  2000-11-22       Impact factor: 11.025

2.  Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly.

Authors:  Laura A Lettice; Taizo Horikoshi; Simon J H Heaney; Marijke J van Baren; Herma C van der Linde; Guido J Breedveld; Marijke Joosse; Nurten Akarsu; Ben A Oostra; Naoto Endo; Minoru Shibata; Mikio Suzuki; Eiichi Takahashi; Toshikatsu Shinka; Yutaka Nakahori; Dai Ayusawa; Kazuhiko Nakabayashi; Stephen W Scherer; Peter Heutink; Robert E Hill; Sumihare Noji
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-28       Impact factor: 11.205

3.  Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting Lmbr1.

Authors:  R M Clark; P C Marker; E Roessler; A Dutra; J C Schimenti; M Muenke; D M Kingsley
Journal:  Genetics       Date:  2001-10       Impact factor: 4.562
  3 in total

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