Literature DB >> 19610119

Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24.

Yvonne Hilhorst-Hofstee1, Zeynep Tümer, Peter Born, Jeroen Knijnenburg, Kerstin Hansson, Vindhya Yatawara, Jesper Steensberg, Reinhard Ullmann, Ger Arkesteijn, Niels Tommerup, Lars Allan Larsen.   

Abstract

Entities:  

Mesh：

Year:  2009        PMID： 19610119     DOI： 10.1002/ajmg.a.32977

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


× No keyword cloud information.
  1 in total

1.  Common Variable Immunodeficiency and Neurodevelopmental Delay Due to a 13Mb Deletion on Chromosome 4 Including the NFKB1 Gene: A Case Report.

Authors:  Clara Franco-Jarava; Irene Valenzuela; Jacques G Riviere; Marina Garcia-Prat; Mónica Martínez-Gallo; Romina Dieli-Crimi; Neus Castells; Laura Batlle-Masó; Pere Soler-Palacin; Roger Colobran
Journal:  Front Immunol       Date:  2022-06-17       Impact factor: 8.786
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.