Genome-wide testing: Genomic medicine

被引:0
作者
McGhee, Sean A.
McCabe, Edward R. B.
机构
[1] Univ Calif Los Angeles, Dept Pediat, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Mater Childrens Hosp, Ctr Soc & Genet, Los Angeles, CA 90095 USA
关键词
D O I
10.1203/01.pdr.0000233116.85413.cd
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:243 / 244
页数:2
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共 14 条
  • [1] Array-based comparative genome hybridization in clinical genetics
    Bar-Shira, Anat
    Rosner, Guy
    Rosner, Serena
    Goldstein, Myriam
    Orr-Urtreger, Avi
    [J]. PEDIATRIC RESEARCH, 2006, 60 (03) : 353 - 358
  • [2] Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: Is less more?
    Bejjani, BA
    Saleki, R
    Ballif, BC
    Rorem, EA
    Sundin, K
    Theisen, A
    Kashork, CD
    Shaffer, LG
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 134A (03) : 259 - 267
  • [3] Detection of gene copy number changes in CGH microarrays using a spatially correlated mixture model
    Broët, P
    Richardson, S
    [J]. BIOINFORMATICS, 2006, 22 (08) : 911 - 918
  • [4] Development and validation of a CGH microarray for clinical cytogenetic diagnosis
    Cheung, SW
    Shaw, CA
    Yu, W
    Li, JZ
    Ou, ZS
    Patel, A
    Yatsenko, SA
    Cooper, ML
    Furman, P
    Stankiewicz, P
    Lupski, JR
    Chinault, AC
    Beaudet, AL
    [J]. GENETICS IN MEDICINE, 2005, 7 (06) : 422 - 432
  • [5] Structural variation in the human genome
    Feuk, L
    Carson, AR
    Scherer, SW
    [J]. NATURE REVIEWS GENETICS, 2006, 7 (02) : 85 - 97
  • [6] GUHA S, 2006, BAYESIAN HIDDEN MARK
  • [7] Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data
    Lai, WR
    Johnson, MD
    Kucherlapati, R
    Park, PJ
    [J]. BIOINFORMATICS, 2005, 21 (19) : 3763 - 3770
  • [8] Chromosomal microdeletions:: Dissecting del22q11 syndrome
    Lindsay, EA
    [J]. NATURE REVIEWS GENETICS, 2001, 2 (11) : 858 - 868
  • [9] Translational genomics in medical genetics
    McCabe, ERB
    [J]. GENETICS IN MEDICINE, 2002, 4 (06) : 468 - 471
  • [10] Dual multiple change-point model leads to more accurate recombination detection
    Minin, VN
    Dorman, KS
    Fang, F
    Suchard, MA
    [J]. BIOINFORMATICS, 2005, 21 (13) : 3034 - 3042