Literature DB >> 9541108

A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation.

S R Ghaffari1, E Boyd, J L Tolmie, Y J Crow, A H Trainer, J M Connor.   

Abstract

Cryptic unbalanced chromosome rearrangements in the telomeric bands of human chromosomes constitute a significant cause of "idiopathic" mental retardation. Here, we have described a new strategy based upon comparative genomic hybridisation (CGH) to screen for these abnormalities. A modified CGH analysis showed three unbalanced cryptic rearrangements in five patients from three families. These chromosome abnormalities and their balanced forms in the relatives were then confirmed by fluorescence in situ hybridisation (FISH). This study describes a new approach to the diagnosis of cryptic translocations between the G band negative ends of chromosomes and confirms the significant contribution of cryptic telomeric rearrangements to idiopathic mental retardation.

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Year:  1998        PMID: 9541108      PMCID: PMC1051247          DOI: 10.1136/jmg.35.3.225

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  33 in total

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Authors:  M R Speicher; S Gwyn Ballard; D C Ward
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2.  Detection of a familial cryptic translocation by fluorescent in situ hybridisation.

Authors:  D P Smith; M Floyd; B Say
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3.  Multicolor spectral karyotyping of human chromosomes.

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Journal:  Science       Date:  1996-07-26       Impact factor: 47.728

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Journal:  Dev Med Child Neurol       Date:  1997-02       Impact factor: 5.449

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Authors:  M Yeargin-Allsopp; C C Murphy; J F Cordero; P Decouflé; J G Hollowell
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6.  Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study.

Authors:  E Reid; N Morrison; L Barron; E Boyd; A Cooke; D Fielding; J L Tolmie
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

7.  Miller-Dieker syndrome due to maternal cryptic translocation t(10;17) (q26.3;p13.3)

Authors:  M Masuno; K Imaizumi; M Nakamura; K Matsui; A Goto; Y Kuroki
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8.  Prenatal and postnatal investigation of a case with Miller-Dieker syndrome due to a familial cryptic translocation t(17;20) (p13.3;q13.3) detected by fluorescence in situ hybridization.

Authors:  S L van Zelderen-Bhola; E J Breslau-Siderius; G C Beverstock; I Stolte-Dijkstra; L S de Vries; P Stoutenbeek; J M de Pater
Journal:  Prenat Diagn       Date:  1997-02       Impact factor: 3.050

9.  Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype.

Authors:  M Erdel; H C Duba; I Verdorfer; A Lingenhel; R Geiger; K H Gutenberger; E Ludescher; B Utermann; G Utermann
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10.  The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation.

Authors:  J Flint; A O Wilkie; V J Buckle; R M Winter; A J Holland; H E McDermid
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Journal:  Genome Res       Date:  2004-02       Impact factor: 9.043

Review 3.  Telomeres: a diagnosis at the end of the chromosomes.

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6.  "Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements.

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7.  Detection of chromosomal aberrations by a whole-genome microsatellite screen.

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Review 8.  Recurrence risks in mental retardation.

Authors:  Y J Crow; J L Tolmie
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  10 in total

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