Literature DB >> 9761395

Polymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders.

G E Hollway1, J C Mulley.   

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Year:  1998        PMID: 9761395     DOI: 10.1111/j.1399-0004.1998.tb03719.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


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  1 in total

1.  Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.

Authors:  P A Jezewski; A R Vieira; C Nishimura; B Ludwig; M Johnson; S E O'Brien; S Daack-Hirsch; R E Schultz; A Weber; B Nepomucena; P A Romitti; K Christensen; I M Orioli; E E Castilla; J Machida; N Natsume; J C Murray
Journal:  J Med Genet       Date:  2003-06       Impact factor: 6.318

  1 in total

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