Literature DB >> 4132492

Letter: Renpenning's syndrome.

M W Steele, A L Chorazy.   

Abstract

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Mesh：

Year:  1974        PMID： 4132492     DOI： 10.1016/s0140-6736(74)92978-x

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

1.  Renpenning syndrome maps to Xp11.

Authors:  R E Stevenson; J F Arena; E Ouzts; A Gibson; M H Shokeir; C Vnencak-Jones; H A Lubs; M May; C E Schwartz
Journal:  Am J Hum Genet       Date:  1998-05       Impact factor: 11.025

2.  Further delineation of X-linked mental retardation.

Authors:  D S Herbst; H G Dunn; F J Dill; D K Kalousek; L W Krywaniuk
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

3.  Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly.

Authors:  Claus Lenski; Fatima Abidi; Alfons Meindl; Alice Gibson; Matthias Platzer; R Frank Kooy; Herbert A Lubs; Roger E Stevenson; Juliane Ramser; Charles E Schwartz
Journal:  Am J Hum Genet       Date:  2004-04       Impact factor: 11.025
  3 in total

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