Literature DB >> 9108874

Conotruncal heart defects and chromosome 22q11 microdeletion.

M C Digilio, B Marino, A Giannotti, G Novelli, B Dallapiccola.   

Abstract

Entities:  

Mesh：

Year:  1997        PMID： 9108874     DOI： 10.1016/s0022-3476(97)70260-9

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


× No keyword cloud information.
  2 in total

Review 1.  22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects.

Authors:  Carolina Putotto; Flaminia Pugnaloni; Marta Unolt; Stella Maiolo; Matteo Trezzi; Maria Cristina Digilio; Annapaola Cirillo; Giuseppe Limongelli; Bruno Marino; Giulio Calcagni; Paolo Versacci
Journal:  Children (Basel)       Date:  2022-05-25

2.  Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome).

Authors:  Mc Digilio; B Marino; R Capolino; B Dallapiccola
Journal:  Images Paediatr Cardiol       Date:  2005-04
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.