Literature DB >> 19396828

Array CGH ends diagnostic odyssey for infant with features of Williams and Alagille syndrome.

C Honeywell, L Gardin, C Jimenez-Rivera, J Allanson.   

Abstract

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Year:  2009        PMID： 19396828     DOI： 10.1002/ajmg.a.32819

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  2 in total

1.  Williams syndrome presenting with findings consistent with Alagille syndrome.

Authors:  Pankaj Sakhuja; Hilary Whyte; Binita Kamath; Nicole Martin; David Chitayat
Journal:  Clin Case Rep       Date:  2014-11-07

2.  Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams' syndrome patients in Saudi Arabia.

Authors:  A Magbooli; E Huwait; A Chaudhary; R Bader; M Gari; F Ashgan; M Alquaiti; A Abuzenadah; M AlQahtani; I R Hussein
Journal:  Mol Cytogenet       Date:  2016-08-12       Impact factor: 2.009
  2 in total

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