Literature DB >> 22051689

Regarding cancer predisposition detected by CHG arrays.

Debra L Collins, R Neil Schimke.   

Abstract

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Year:  2011        PMID： 22051689     DOI： 10.1097/gim.0b013e31823552a8

Source DB:  PubMed          Journal:  Genet Med        ISSN： 1098-3600            Impact factor:   8.822


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  2 in total

Review 1.  Contiguous gene deletion of chromosome 2p16.3-p21 as a cause of Lynch syndrome.

Authors:  Erin E Salo-Mullen; Patricio B Lynn; Lu Wang; Michael Walsh; Anuradha Gopalan; Jinru Shia; Christina Tran; Fung Ying Man; Sean McBride; Mark Schattner; Liying Zhang; Martin R Weiser; Zsofia K Stadler
Journal:  Fam Cancer       Date:  2018-01       Impact factor: 2.375

2.  Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphoma.

Authors:  N van Engelen; F van Dijk; E Waanders; A Buijs; M A Vermeulen; J L C Loeffen; R P Kuiper; M C J Jongmans
Journal:  Fam Cancer       Date:  2021-04-03       Impact factor: 2.375
  2 in total

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