Literature DB >> 3239570

Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes).

R M Winter1, S M Huson.   

Abstract

Greig cephalopolysyndactyly syndrome is an autosomal dominant form of complex polydactyly in man. Attention is called to the evidence that, on both morphological and comparative gene mapping grounds, this defect is homologous to Xt-extra toes in the mouse. The pattern of polydactyly in both species is very similar. In addition, both conditions probably map close to the T-cell receptor gamma polypeptide at 13 A2-3 in mouse and 7p15 in humans.

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Year:  1988        PMID： 3239570     DOI： 10.1002/ajmg.1320310411

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


  11 in total

1.  Why study human limb malformations?

Authors:  Andrew O M Wilkie
Journal:  J Anat       Date:  2003-01       Impact factor: 2.610

Review 2.  Current perspectives on the genetic causes of neural tube defects.

Authors:  Patrizia De Marco; Elisa Merello; Samantha Mascelli; Valeria Capra
Journal:  Neurogenetics       Date:  2006-08-29       Impact factor: 2.660

Review 3.  Mapping dysmorphic syndromes with the aid of the human/mouse homology map.

Authors:  R P Erickson
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

4.  The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling.

Authors:  Derek E Gildea; Erin S Luetkemeier; Xiaozhong Bao; Stacie K Loftus; Susan Mackem; Yingzi Yang; William J Pavan; Leslie G Biesecker
Journal:  FASEB J       Date:  2011-02-03       Impact factor: 5.191

Review 5.  Dysmorphic disorders--an overview.

Authors:  D Donnai
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

6.  The acrocallosal syndrome and Greig syndrome are not allelic disorders.

Authors:  L A Brueton; K A Chotai; L van Herwerden; A Schinzel; R M Winter
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

7.  The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3.

Authors:  T Schimmang; S I Oda; U Rüther
Journal:  Mamm Genome       Date:  1994-06       Impact factor: 2.957

8.  Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt).

Authors:  A Vortkamp; T Franz; M Gessler; K H Grzeschik
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

9.  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

10.  Isolation and characterization of a cosmid contig for the GCPS gene region.

Authors:  A Vortkamp; C Heid; M Gessler; K H Grzeschik
Journal:  Hum Genet       Date:  1995-01       Impact factor: 4.132
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