Literature DB >> 22302716

A small terminal deletion 11q in a boy without Jacobsen syndrome: narrowing the critical region for the 11q Jacobsen syndrome phenotype.

Christina Evers1, Johannes W G Janssen, Anna Jauch, Michael Bonin, Ute Moog.   

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Year:  2012        PMID： 22302716     DOI： 10.1002/ajmg.a.34433

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


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  1 in total

1.  Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up.

Authors:  Vera Ayres Meloni; Sylvia Satomi Takeno; Ana Luiza Pilla; Claudia Berlim de Mello; Maria Isabel Melaragno; Leslie Domenici Kulikowski
Journal:  Mol Cytogenet       Date:  2014-08-22       Impact factor: 2.009
  1 in total

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