Literature DB >> 2014804

Concurrence of dominant piebald trait and fragile X syndrome.

B Finucane, C I Scott, M B Kurtz.   

Abstract

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Year:  1991        PMID： 2014804      PMCID： PMC1682941     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  1 in total

1.  Dominant piebald trait (white forelock and leukoderma) with neurological impairment.

Authors:  M A Telfer; M Sugar; E A Jaeger; J Mulcahy
Journal:  Am J Hum Genet       Date:  1971-07       Impact factor: 11.025
  1 in total
  1 in total

1.  Human piebald trait resulting from a dominant negative mutant allele of the c-kit membrane receptor gene.

Authors:  R A Fleischman
Journal:  J Clin Invest       Date:  1992-06       Impact factor: 14.808
  1 in total

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