46,XY, der(3)t(1;3)(q23;p22)

Double aneuploidy at a new breakpoint

S. N. Joshi, A. Ganesh, P. Venugopalan

Research output: Contribution to journalArticle

Abstract

A 12-month-old Omani boy is described with double aneuploidy involving chromosomes 1 and 3. In this case the aberration involved segment (q23;p22) which has not been reported previously.

Original languageEnglish
Pages (from-to)145-146
Number of pages2
JournalClinical Dysmorphology
Volume11
Issue number2
Publication statusPublished - 2002

Fingerprint

Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 1
Aneuploidy

Keywords

  • Chromosome aberration
  • Partial monosomy 3p
  • Partial trisomy 1q
  • Translocation 1;3

ASJC Scopus subject areas

  • Genetics(clinical)
  • Pediatrics, Perinatology, and Child Health
  • Anatomy

Cite this

46,XY, der(3)t(1;3)(q23;p22) : Double aneuploidy at a new breakpoint. / Joshi, S. N.; Ganesh, A.; Venugopalan, P.

In: Clinical Dysmorphology, Vol. 11, No. 2, 2002, p. 145-146.

Research output: Contribution to journalArticle

Joshi, SN, Ganesh, A & Venugopalan, P 2002, '46,XY, der(3)t(1;3)(q23;p22): Double aneuploidy at a new breakpoint', Clinical Dysmorphology, vol. 11, no. 2, pp. 145-146.
Joshi, S. N. ; Ganesh, A. ; Venugopalan, P. / 46,XY, der(3)t(1;3)(q23;p22) : Double aneuploidy at a new breakpoint. In: Clinical Dysmorphology. 2002 ; Vol. 11, No. 2. pp. 145-146.
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