Literature DB >> 4142400

Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.

Y E Hsia, V Appadorai, W R Breg, R O Howard.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1974        PMID： 4142400

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


× No keyword cloud information.
  2 in total

1.  The Meckel Syndrome. Pathological and cytogenetic observations in eight cases.

Authors:  P Moerman; E Verbeken; J P Fryns; P Goddeeris; J M Lauweryns
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

2.  Ring chromosome 3 in a retarded boy.

Authors:  R Witkowski; E Ullrich; U Piede
Journal:  Hum Genet       Date:  1978-06-27       Impact factor: 4.132
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.