Literature DB >> 2901328

Molecular studies of the parental origin and nature of human X isochromosomes.

M Harbison1, T Hassold, C Kobryn, P A Jacobs.   

Abstract

X-chromosome restriction fragment length polymorphisms were used to determine the parental origin of the isochromosome in nine individuals with an i(Xq) or idic(Xq). We were able to specify the parental source of eight of the nine isochromosomes, with six being maternal and two paternal in origin. In two cases, one i(Xq) and one idic(Xq), we used Xq markers to determine the level of heterozygosity in the isochromosome. Each was homozygous at all tested loci, suggesting that each originated from a single X chromosome and not from an exchange of material between two X's.

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Year:  1988        PMID: 2901328     DOI: 10.1159/000132553

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  7 in total

1.  Analysis of the origin of Turner's syndrome using polymorphic DNA probes.

Authors:  S A Loughlin; A Redha; J McIver; E Boyd; A Carothers; J M Connor
Journal:  J Med Genet       Date:  1991-03       Impact factor: 6.318

2.  Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.

Authors:  Stuart A Scott; Ninette Cohen; Tracy Brandt; Peter E Warburton; Lisa Edelmann
Journal:  Hum Mol Genet       Date:  2010-06-22       Impact factor: 6.150

3.  A molecular study of X isochromosomes: parental origin, centromeric structure, and mechanisms of formation.

Authors:  I Lorda-Sanchez; F Binkert; M Maechler; A Schinzel
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

4.  Molecular and cytogenetic analysis of a familial microdeletion of Xq.

Authors:  S Wells; S Mould; D Robins; D Robinson; P Jacobs
Journal:  J Med Genet       Date:  1991-03       Impact factor: 6.318

5.  Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity.

Authors:  C B Sharp; H M Bedford; H F Willard
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

6.  Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.

Authors:  D J Wolff; A P Miller; D L Van Dyke; S Schwartz; H F Willard
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

7.  Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.

Authors:  F A Eggerding; S A Schonberg; F F Chehab; M E Norton; V A Cox; C J Epstein
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

  7 in total

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