Literature DB >> 13778772

[Congenital human anomalies caused by chromosomal aberrations].

R TURPIN, J LEJEUNE.   

Abstract

Entities:  

Keywords:  ABNORMALITIES/etiology; CHROMOSOMES

Mesh：

Year:  1961        PMID： 13778772

Source DB:  PubMed          Journal:  Maandschr Kindergeneeskd        ISSN： 0024-869X


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  2 in total

1.  [ON A FAMILIAL DISEASE WITH AN UNUSUAL NEUROLOGIC SYMPTOM COMBINATION, OLIGOPHRENIA, DEMENTIA, MULTIPLE SKIN ULCERATIONS, SPLENOMEGALY AND AMINO ACID METABOLIC DISORDERS].

Authors:  J BRUCK; F GERSTENBRAND; P PROSENZ; R SANTLER; B SCHOBEL; F WEWALKA
Journal:  Dtsch Z Nervenheilkd       Date:  1964-02-21

2.  A Search for Ocular Anomalies in Persons with Abnormal Numbers of Sex Chromosomes.

Authors:  C McCulloch; W S Hunter
Journal:  Can Med Assoc J       Date:  1962-01-06       Impact factor: 8.262
  2 in total

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