Two infants with del(3)(p25pter) and a review of previously reported cases

Jeanette Ramer, Roger Ladda, C. Frankel

Research output: Contribution to journalReview articlepeer-review

19 Scopus citations

Abstract

Del(3)(p25pter) is associated with a characteristic multiple congenital anomalies/mental retardation syndrome. Early recognition of these manifestations and identification of the chromosome defect are essential for proper management and counseling.

Original languageEnglish (US)
Pages (from-to)108-112
Number of pages5
JournalAmerican Journal of Medical Genetics
Volume33
Issue number1
DOIs
StatePublished - Jan 1 1989

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

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