Literature DB >> 2012130

Routine use of methods for improved G-band resolution in a population of patients with malformations and developmental delay.

J T Mascarello1, V Hubbard.   

Abstract

We report on an 11-year experience in which cell culture synchronization and other methods for improving cytogenetic detail were used to study 2,245 patients presenting with malformations and (usually) developmental delay. Not including patients presenting with one of the so-called "contiguous gene syndromes," 30 patients (1.1% of the study population) were found to have karyotypes characterized by structural alterations that were either subtle enough to be judged undetectable in standard metaphase preparations or subtle enough to have escaped detection in previous banded studies. Analysis of the detail available for 6 chromosome pairs suggests that the average banding detail available for these analyses fell short of that considered to be "high-resolution" but was, nevertheless, more than would have been expected from standard metaphase preparations.

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Year:  1991        PMID: 2012130     DOI: 10.1002/ajmg.1320380110

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


  7 in total

1.  Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

Authors:  J C Barber; C A Joyce; M N Collinson; J C Nicholson; L R Willatt; H M Dyson; M S Bateman; A J Green; J R Yates; N R Dennis
Journal:  J Med Genet       Date:  1998-06       Impact factor: 6.318

2.  Investigation of a patient with a partial trisomy 16q including the fat mass and obesity associated gene (FTO): fine mapping and FTO gene expression study.

Authors:  Linda van den Berg; Henriette Delemarre-van de Waal; Joan C Han; Bauke Ylstra; Paul Eijk; Maria Nesterova; Peter Heutink; Constantine A Stratakis
Journal:  Am J Med Genet A       Date:  2010-03       Impact factor: 2.802

Review 3.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

Review 4.  Chromosome abnormalities without phenotypic consequences.

Authors:  Małgorzata Kowalczyk; Małgorzata Srebniak; Agnieszka Tomaszewska
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

5.  Novel duplication on chromosome 16 (q12.1-q21) associated with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case report.

Authors:  Ljubica Odak; Ingeborg Barisić; Leona Morozin Pohovski; Mariluce Riegel; Albert Schinzel
Journal:  Croat Med J       Date:  2011-06       Impact factor: 1.351

6.  A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1-q12.1 in a healthy man.

Authors:  Laura Rodríguez; Tomas Liehr; María Luisa Martínez-Fernández; Ana Lara; Antonio Torres; María Luisa Martínez-Frías
Journal:  Mol Cytogenet       Date:  2008-04-02       Impact factor: 2.009

7.  A Very Rare Partial Trisomy Syndrome: De Novo Duplication of 16q12.1q23.3 in a Turkish Girl with Developmental Delay and Facial Dysmorphic Features.

Authors:  A Türkyılmaz; O Yaralı
Journal:  Balkan J Med Genet       Date:  2020-08-26       Impact factor: 0.519

  7 in total

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