Literature DB >> 21790733

Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasia.

M Pavlovsky, D Fuchs-Telem, J Nousbeck, O Sarig, E Sprecher.   

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Year:  2011        PMID： 21790733     DOI： 10.1111/j.1365-2230.2011.04135.x

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN： 0307-6938            Impact factor:   3.470


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  2 in total

1.  Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study.

Authors:  Sigrun Wohlfart; Ralph Meiller; Johanna Hammersen; Jung Park; Johannes Menzel-Severing; Volker O Melichar; Kenneth Huttner; Ramsey Johnson; Florence Porte; Holm Schneider
Journal:  Orphanet J Rare Dis       Date:  2020-01-10       Impact factor: 4.123

2.  No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.

Authors:  Laura Körber; Holm Schneider; Nicole Fleischer; Sigrun Maier-Wohlfart
Journal:  Orphanet J Rare Dis       Date:  2021-02-23       Impact factor: 4.123
  2 in total

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