Literature DB >> 26100565

Hypogammaglobulinemia and impaired antibody response in a child with chromosome 2p15-16.1 microdeletion syndrome.

Katherine M Ottolini1, Clesson E Turner2, Satyen M Gada3.   

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Year:  2015        PMID： 26100565     DOI： 10.1016/j.anai.2015.05.016

Source DB:  PubMed          Journal:  Ann Allergy Asthma Immunol        ISSN： 1081-1206            Impact factor:   6.347


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  2 in total

1.  Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.

Authors:  Hani Bagheri; Chansonette Badduke; Ying Qiao; Rita Colnaghi; Iga Abramowicz; Diana Alcantara; Christopher Dunham; Jiadi Wen; Robert S Wildin; Malgorzata Jm Nowaczyk; Jennifer Eichmeyer; Anna Lehman; Bruno Maranda; Sally Martell; Xianghong Shan; Suzanne Me Lewis; Mark O'Driscoll; Cheryl Y Gregory-Evans; Evica Rajcan-Separovic
Journal:  JCI Insight       Date:  2016-03-17

2.  Haploinsufficiency of BCL11A associated with cerebellar abnormalities in 2p15p16.1 deletion syndrome.

Authors:  Hiroko Shimbo; Takayuki Yokoi; Noriko Aida; Seiji Mizuno; Hiroshi Suzumura; Junichi Nagai; Kazumi Ida; Yumi Enomoto; Chihiro Hatano; Kenji Kurosawa
Journal:  Mol Genet Genomic Med       Date:  2017-05-22       Impact factor: 2.183
  2 in total

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