Literature DB >> 13868059

[Current orientation of chromosomal explorations in congenital encephalopathies with complex dysmorphia. (Apropos of 13 cases)].

R BERNARD, A STAHL, F GIRAUD.   

Abstract

Entities:  

Keywords:  ABNORMALITIES/genetics; BRAIN/diseases; CHROMOSOMES; MONGOLISM/genetics

Mesh：

Year:  1962        PMID： 13868059

Source DB:  PubMed          Journal:  Mars Med        ISSN： 0025-4053


× No keyword cloud information.
  1 in total

1.  The Cornelia de Lange syndrome: clinical and cytogenetic interpretations.

Authors:  H W Payne; W K Maeda
Journal:  Can Med Assoc J       Date:  1965-09-11       Impact factor: 8.262
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.