Literature DB >> 11746026

De novo inverted tandem duplication of the short arm of chromosome 12 in a patient with microblepharon.

M Tekin1, C Jackson-Cook, A Pandya.   

Abstract

We present a patient with a de novo inverted duplication of nearly the entire short arm of chromosome 12 [inv dup(12)(p13.3p12)], which was characterized using GTG-banding and spectral karyotyping. The patient was noted to have microblepharon, which has not been previously described in children with a similar chromosomal rearrangement. This patient represents one of the few examples of complete and pure trisomy 12p due to inverted duplication of the short arm of chromosome 12 and expands the clinical spectrum. Copyright 2001 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2001        PMID: 11746026     DOI: 10.1002/ajmg.10025

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

1.  Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).

Authors:  D A Koolen; W M Nillesen; M H A Versteeg; G F M Merkx; N V A M Knoers; M Kets; S Vermeer; C M A van Ravenswaaij; C G de Kovel; H G Brunner; D Smeets; B B A de Vries; E A Sistermans
Journal:  J Med Genet       Date:  2004-12       Impact factor: 6.318

2.  Non-mosaic partial duplication 12p in a patient with dysmorphic characteristics and developmental delay.

Authors:  Jakeline Santos Oliveira; Tatiana Mozer Joaquim; Rosana Aparecida Bicudo da Silva; Deise Helena de Souza; Lúcia Regina Martelli; Danilo Moretti-Ferreira
Journal:  Genet Mol Biol       Date:  2020-02-10       Impact factor: 1.771

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.