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, David Weaver, M. E. Hodes

Research output: Contribution to journalArticle

10 Citations (Scopus)

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 - 1982
Externally publishedYes

Fingerprint

Sternum
Diaphragmatic Hernia
Ventricular Heart Septal Defects
Cleft Palate
Ribs
Karyotype
Cytogenetics
Intellectual Disability
Growth
Chromosome 4q- Syndrome

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

Brief cytogenetic case report : A 4.5-year-old girl with deletion 4q syndrome - De novo, 46,XX, del(4) (pter→q31:). / Young, R. S.; Palmer, C. G.; Bender, H. A.; Weaver, David; Hodes, M. E.

In: American Journal of Medical Genetics, Vol. 12, No. 1, 1982, p. 103-107.

Research output: Contribution to journalArticle

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