Literature DB >> 10637567

Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome.

G Novelli, F Amati, B Dallapiccola.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2000        PMID： 10637567     DOI： 10.1016/s1357-4310(99)01577-4

Source DB:  PubMed          Journal:  Mol Med Today        ISSN： 1357-4310


× No keyword cloud information.
  2 in total

1.  Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome.

Authors:  Katrina Prescott; Sarah Ivins; Mike Hubank; Elizabeth Lindsay; Antonio Baldini; Peter Scambler
Journal:  Hum Genet       Date:  2005-03-19       Impact factor: 4.132

2.  Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Authors:  M Pierdominici; F Mazzetta; E Caprini; M Marziali; M C Digilio; B Marino; A Aiuti; F Amati; G Russo; G Novelli; F Pandolfi; G Luzi; A Giovannetti
Journal:  Clin Exp Immunol       Date:  2003-05       Impact factor: 4.330
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.