Literature DB >> 5600521

[A very rare case of Klinefelter syndrome with XXXXY (2n-49) chromosome constitution].

A G Gedikoğlu.   

Abstract

Entities:  

Mesh:

Year:  1967        PMID: 5600521

Source DB:  PubMed          Journal:  Tip Fak Mecm


× No keyword cloud information.
  1 in total

1.  XXXXY syndrome in a phenotypic male infant with associated cardiac abnormalities.

Authors:  S R Assemany; R L Neu; L I Gardner
Journal:  Humangenetik       Date:  1971
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.