Literature DB >> 1475257

Prenatal diagnosis of terminal deletion 1 (q42)

B Dallapiccola, G Ferranti, A Pachì.   

Abstract

Mesh：

Year:  1992        PMID： 1475257     DOI： 10.1002/pd.1970121014

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  2 in total

1.  Prenatal diagnosis of a terminal chromosome 1 (q42-q44) deletion: original case report and review of the literature.

Authors:  C Van Linthout; V Emonard; J S Gatot; X Capelle; F Kridelka; P Emonts; M C Segghaye
Journal:  Facts Views Vis Obgyn       Date:  2016-06-27

2.  Constitutional 763.3 Kb chromosome 1q43 duplication encompassing only CHRM3 gene identified by next generation sequencing (NGS) in a child with intellectual disability.

Authors:  Xiaofei Cheng; Qifang Yang; Jun Liu; Juan Ye; Huiying Xiao; Gaimei Zhang; Yuanyuan Pan; Xia Li; Ruifeng Hao; Yinfeng Li
Journal:  Mol Cytogenet       Date:  2019-04-17       Impact factor: 2.009
  2 in total

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