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unlvlibraries' limk1 [1 article]

Artikler nylig sendt til unlvlibraries' bibliotek klassifisert med nøkkelordet limk1. You can also see everyone's limk1.
  • notes GTF2I hemizygosity implicated in mental retardation in Williams syndrome: Genotype-phenotype analysis of five families with deletions in the Williams syndrome region
    American Journal of Medical Genetics Part A, Vol. 123A, No. 1. (17 September 2003), pp. 45-59.
    by Colleen A Morris, Carolyn B Mervis, Holly H Hobart, Ronald G Gregg, Jacquelyn Bertrand, Gregory J Ensing, Annemarie Sommer, Cynthia A Moore, Robert J Hopkin, Patricia A Spallone, Mark T Keating, Lucy Osborne, Kendra W Kimberley, Dean D Stock
    posted to 7q1123 aortic correlation deletion eln genetics genotype-phenotype gtf2i limk1 pediatrics stenosis supravalvar syndrome williams by unlvlibraries on 2005-03-29 20:10:41 as **
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