Literature DB >> 8117067

Familial pericentric inversion of chromosome 13, 46,XX,inv (13)(p13;q11): a new variant.

F M Mohammed1, D S Krishna Murthy, T I Farag, S A al-Awadi, S A al-Othman, I Hammad.   

Abstract

A 10-year-old female with right oblique inguinal hernia was investigated to exclude an XY karyotype. Chromosome analysis of peripheral blood showed 46,XX,inv(13)(p13;q11). In vitro aneuploidy was observed in two cells: a) 46,XX,inv(13), inv(13); b) 47,XX, +inv(13). Her father and three sisters were carriers for inv(13). Herein the authors review briefly familial inv(13)'s and report a new variant involving breakpoints (p13;q11).

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Year:  1993        PMID: 8117067

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  2 in total

1.  Kabuki syndrome-like features in monozygotic twin boys with a pseudodicentric chromosome 13.

Authors:  S A Lynch; K A Ashcroft; S Zwolinski; C Clarke; J Burn
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

2.  Structural chromosomal anomaly in mental retardation.

Authors:  K S Reddy; S Rajangam; I M Thomas
Journal:  Indian J Pediatr       Date:  1999 Nov-Dec       Impact factor: 1.967

  2 in total

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