Literature DB >> 8839733

Terminal deletion of chromosome 1--a recognizable condition.

J Schefels, E Keller-Röttger, K J Esser.   

Abstract

Mesh：

Year:  1996        PMID： 8839733     DOI： 10.1007/bf01957161

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  4 in total

Review 1.  A specific syndrome due to deletion of the distal long arm of chromosome 1.

Authors:  P Meinecke; D Vögtel
Journal:  Am J Med Genet       Date:  1987-10

2.  Chromosome 1q terminal deletion resulting from de novo translocation with an acrocentric chromosome.

Authors:  E Arai; S Nishimura; K Tamura; M Kida; T Ikeuchi
Journal:  Jpn J Hum Genet       Date:  1994-12

3.  [Distal 1q monosomy. 2 new cases and description of the syndrome].

Authors:  C Turleau; J de Grouchy; J Frézal; J M Richardet
Journal:  Ann Genet       Date:  1983

4.  Deletion of the distal long arm of chromosome 1: a definable syndrome.

Authors:  V P Johnson; L J Heck; G A Carter; J O Flom
Journal:  Am J Med Genet       Date:  1985-12
  4 in total
  1 in total

1.  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
  1 in total

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