Literature DB >> 17910074

Novel microdeletion syndromes.

Ian D Krantz1, Nancy B Spinner.   

Abstract

Mesh：

Year:  2007        PMID： 17910074     DOI： 10.1002/ajmg.c.30150

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN： 1552-4868            Impact factor:   3.908


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  1 in total

1.  A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability.

Authors:  J R M Ceroni; R L Dutra; R S Honjo; J C Llerena; A X Acosta; P F V Medeiros; M F Galera; É A Zanardo; F B Piazzon; A T Dias; G M Novo-Filho; M M Montenegro; F A R Madia; D R Bertola; J B de Melo; L D Kulikowski; C A Kim
Journal:  Sci Rep       Date:  2018-09-06       Impact factor: 4.379
  1 in total

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