Chromosome 10qter deletion syndrome: A review and report of three new cases

E. A. Wulfsberg, P. Weaver, C. M. Cunniff, M. C. Jones, K. L. Jones

Research output: Contribution to journalReview articlepeer-review

58 Scopus citations

Abstract

We report on three patients with terminal deletions of chromosome 10q and compare them to 15 previously reported patients. A similar facial appearance with a prominent beaked nose, large and/or malformed ears, and a pattern of major abnormalities including severe mental retardation, cardiac anomalies, and anogenital anomalies are reviewed. We feel the manifestation of del 10qter are sufficiently distinct to suggest this diagnosis on clinical examination.

Original languageEnglish (US)
Pages (from-to)364-367
Number of pages4
JournalAmerican journal of medical genetics
Volume32
Issue number3
DOIs
StatePublished - Jan 1 1989

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Fingerprint Dive into the research topics of 'Chromosome 10qter deletion syndrome: A review and report of three new cases'. Together they form a unique fingerprint.

Cite this