Literature DB >> 9268103

Prenatal detection and molecular characterization of a de novo duplication of the distal long arm of chromosome 19.

P D Cotter1, L D McCurdy, I F Gershin, A Babu, J P Willner, R J Desnick.   

Abstract

A tandem duplication of the distal long arm of chromosome 19 was identified in a 10 week fetus by analysis of chorionic villi. The fetal karyotype from two primary cultures was 46,XY,dir dup(19)(q13.2q13.4). The origin of the extra material was confirmed by fluorescence in situ hybridization using a chromosome 19 whole chromosome probe. Parental chromosomes were normal, indicating a de novo origin of the extra chromosome material. This is the first case of dup(19q) detected by prenatal diagnosis. Molecular studies demonstrated that the duplication involved a maternal chromosome 19.

Mesh:

Year:  1997        PMID: 9268103     DOI: 10.1002/(sici)1096-8628(19970822)71:3<325::aid-ajmg13>3.0.co;2-m

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


  3 in total

1.  Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications.

Authors:  D Kotzot; M J Martinez; G Bagci; S Basaran; A Baumer; F Binkert; L Brecevic; C Castellan; K Chrzanowska; F Dutly; A Gutkowska; S B Karaüzüm; M Krajewska-Walasek; G Luleci; P Miny; M Riegel; S Schuffenhauer; H Seidel; A Schinzel
Journal:  J Med Genet       Date:  2000-04       Impact factor: 6.318

2.  19q13.33→qter trisomy in a girl with intellectual impairment and seizures.

Authors:  Gianna Carvalheira; Mariana Moysés Oliveira; Sylvia Takeno; Fernanda Teresa de Lima; Vera Ayres Meloni; Maria Isabel Melaragno
Journal:  Meta Gene       Date:  2014-10-27

3.  A Novel 1.13 Mb Interstitial Duplication at 19q13.32 Causing Developmental Delay and Microcephaly in a Pediatric Patient: the First Asian Case Reports.

Authors:  John Hoon Rim; Jeong A Kim; Jongha Yoo
Journal:  Yonsei Med J       Date:  2017-11       Impact factor: 2.759

  3 in total

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