Terminal deletion(4)(q33) in a male infant

J. Stamberg, E. W. Jabs, E. Elias

Research output: Contribution to journalArticlepeer-review

14 Scopus citations


The deletion of 4q31→qter is associated with a recognizable '4q- syndrome'. It has been proposed that the much rarer deletion 4q33→qter causes a milder phenotypic expression of the 4q- syndrome. We present the second case, the first male, with the latter deletion and compare his clinical features to those of other 4q- patients.

Original languageEnglish (US)
Pages (from-to)125-129
Number of pages5
JournalClinical Genetics
Issue number2
StatePublished - 1982

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)


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