Literature DB >> 19921650

Absence of SIX3 mutations in patients with congenital hypopituitarism.

Carles Gaston-Massuet1, Daniel Kelberman, Mehul Dattani, Juan Pedro Martinez-Barbera.   

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Year:  2009        PMID： 19921650     DOI： 10.1002/ajmg.a.33103

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


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  2 in total

1.  Cornelia de Lange Syndrome: NIPBL haploinsufficiency downregulates canonical Wnt pathway in zebrafish embryos and patients fibroblasts.

Authors:  A Pistocchi; G Fazio; A Cereda; L Ferrari; L R Bettini; G Messina; F Cotelli; A Biondi; A Selicorni; V Massa
Journal:  Cell Death Dis       Date:  2013-10-17       Impact factor: 8.469

2.  Copy Number Variants Contributing to Combined Pituitary Hormone Deficiency.

Authors:  Bartłomiej Budny; Katarzyna Karmelita-Katulska; Marek Stajgis; Tomasz Żemojtel; Marek Ruchała; Katarzyna Ziemnicka
Journal:  Int J Mol Sci       Date:  2020-08-11       Impact factor: 5.923
  2 in total

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