Literature DB >> 20466309

Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21 --> q11.23 by array comparative genomic hybridization.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Chin-Yuan Hsu, Chen-Chi Lee, Wayseen Wang.   

Abstract

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Year:  2010        PMID： 20466309     DOI： 10.1016/S1028-4559(10)60025-3

Source DB:  PubMed          Journal:  Taiwan J Obstet Gynecol        ISSN： 1028-4559            Impact factor:   1.705


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  1 in total

1.  A Novel Mutation in NIPBL Gene with the Cornelia de Lange Syndrome and a 10q11.22-q11.23 Microdeletion in the Same Individual.

Authors:  Haydar Bağış; Özden Öztürk; Semih Bolu; Bayram Taşkın
Journal:  J Pediatr Genet       Date:  2020-10-15
  1 in total

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