Literature DB >> 14152037

[FAMILIAL 2 - 22 TRANSLOCATION; ASSOCIATION WITH A HAPLO-X TURNER'S SYNDROME].

J LEJEUNE, J LAFOURCADE, C SALMON, R TURPIN.   

Abstract

Keywords:  BLOOD GROUPS; CHROMOSOME ABNORMALITIES; GENETICS, HUMAN; SALIVA; TURNER'S SYNDROME

Mesh：

Substances：

Year:  1963        PMID： 14152037

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


× No keyword cloud information.
  2 in total

1.  Familial 2/3 translocation.

Authors:  R L Summitt
Journal:  Am J Hum Genet       Date:  1966-03       Impact factor: 11.025

2.  Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1).

Authors:  Z Cetin; I Mendilcioglu; S Yakut; S Berker-Karauzum; B Karaman; G Luleci
Journal:  Balkan J Med Genet       Date:  2011-06       Impact factor: 0.519
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.