Literature DB >> 19253381

Germinal mosaicism of GATA3 in a family with HDR syndrome.

Yue Sun1, Weibo Xia, Xiaoping Xing, Mei Li, Ou Wang, Yan Jiang, Yu Pei, Ping Ye, Huaicheng Liu, Yingying Hu, Xunwu Meng, Xueying Zhou.   

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Year:  2009        PMID： 19253381     DOI： 10.1002/ajmg.a.32706

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  4 in total

1.  GATA3 mutation in a family with hypoparathyroidism, deafness and renal dysplasia syndrome.

Authors:  Zi-Yang Zhu; Qiao-Li Zhou; Shi-Ning Ni; Wei Gu
Journal:  World J Pediatr       Date:  2014-08-15       Impact factor: 2.764

2.  Auditory and vestibular phenotypes associated with GATA3 mutation.

Authors:  Wade Wei-De Chien; Jennifer W Leiding; Amy P Hsu; Christopher Zalewski; Kelly King; Steven M Holland; Carmen Brewer
Journal:  Otol Neurotol       Date:  2014-04       Impact factor: 2.311

3.  The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome.

Authors:  Hakan Döneray; Takeshi Usui; Avni Kaya; Ayşe Sena Dönmez
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-06

4.  A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome.

Authors:  Gül Yeşiltepe Mutlu; Heves Kırmızıbekmez; Akie Nakamura; Maki Fukami; Şükrü Hatun
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-12
  4 in total

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