Literature DB >> 10198173

A 1.5-Mb contig within the cat eye syndrome critical region at human chromosome 22q11.2.

A Johnson1, S Minoshima, S Asakawa, N Shimizu, H Shizuya, B A Roe, H E McDermid.   

Abstract

We have constructed a 1.5-Mb contig spanning the distal half of the critical region for cat eye syndrome on human chromosome 22 from D22S543 to D22S181. The contig consists of 20 P1 artificial chromosome (PAC) clones and 11 bacterial artificial chromosome (BAC) clones screened from 2 BAC and 2 PAC libraries. Continuous overlap between the clones was confirmed using vectorette PCR and riboprobes. Despite the instability of this region in a previous YAC contig, only 1 BAC showed a minor instability and then in only one isolation. This contig is now providing the basis for genomic sequencing and gene identification in the cat eye syndrome critical region. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10198173     DOI: 10.1006/geno.1999.5757

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  Analysis of the cat eye syndrome critical region in humans and the region of conserved synteny in mice: a search for candidate genes at or near the human chromosome 22 pericentromere.

Authors:  T K Footz; P Brinkman-Mills; G S Banting; S A Maier; M A Riazi; L Bridgland; S Hu; B Birren; S Minoshima; N Shimizu; H Pan; T Nguyen; F Fang; Y Fu; L Ray; H Wu; S Shaull; S Phan; Z Yao; F Chen; A Huan; P Hu; Q Wang; P Loh; S Qi; B A Roe; H E McDermid
Journal:  Genome Res       Date:  2001-06       Impact factor: 9.043

2.  A method for accurate detection of genomic microdeletions using real-time quantitative PCR.

Authors:  Rosanna Weksberg; Simon Hughes; Laura Moldovan; Anne S Bassett; Eva W C Chow; Jeremy A Squire
Journal:  BMC Genomics       Date:  2005-12-13       Impact factor: 3.969

3.  Chromosomal abnormalities and copy number variations in fetal ventricular septal defects.

Authors:  Meiying Cai; Hailong Huang; Linjuan Su; Na Lin; Xiaoqing Wu; Xiaorui Xie; Gang An; Ying Li; Yuan Lin; Liangpu Xu; Hua Cao
Journal:  Mol Cytogenet       Date:  2018-11-28       Impact factor: 2.009

4.  Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome.

Authors:  Meiying Cai; Hailong Huang; Linjuan Su; Na Lin; Xiaoqing Wu; Xiaorui Xie; Gang An; Ying Li; Yuan Lin; Liangpu Xu
Journal:  Medicine (Baltimore)       Date:  2018-12       Impact factor: 1.817

5.  Molecular cytogenetic identification of small supernumerary marker chromosomes using chromosome microarray analysis.

Authors:  Huili Xue; Liangpu Xu; Hailong Huang; Yan Wang; Gang An; Min Zhang; Yuan Lin
Journal:  Mol Cytogenet       Date:  2019-03-11       Impact factor: 2.009

6.  Disorders caused by chromosome abnormalities.

Authors:  Aaron Theisen; Lisa G Shaffer
Journal:  Appl Clin Genet       Date:  2010-12-10
  6 in total

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