Brief cytogenetic case report: A 4.5-year-old girl with deletion 4q syndrome - De novo, 46,XX, del(4) (pter→q31:)

R. S. Young, C. G. Palmer, H. A. Bender, D. D. Weaver, M. E. Hodes

Research output: Contribution to journalArticle

10 Scopus citations

Abstract

A 3.5-year-old white girl had growth and mental retardation of prenatal origin, unusual facial appearance, cleft palate, abnormal sternum, absence or hypoplasia of some digits, diaphragmatic hernia, ventricular septal defect, and rib and vertebral anomalies. Her karyotype was 46,XX,del(4)(pter→q31:).

Original languageEnglish (US)
Pages (from-to)103-107
Number of pages5
JournalAmerican Journal of Medical Genetics
Volume12
Issue number1
DOIs
StatePublished - Jul 13 1982
Externally publishedYes

    Fingerprint

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this