A novel locus for keratoconus on 5q14.3-q21.1

被引：0
|
作者：
Rabinowitz, YS
Tang, Y
Picornell, Y
Taylor, K
Yang, H
机构：
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2005年 / 46卷
关键词：
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
4955
引用
收藏
页数：1
相关论文
共 50 条
  • [1] Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1
    Tang, YMG
    Rabinowitz, YS
    Taylor, KD
    Li, XH
    Hu, MS
    Picornell, Y
    Yang, HY
    GENETICS IN MEDICINE, 2005, 7 (06) : 397 - 405
  • [2] A POLYMORPHIC LOCUS, D10S5, AT 10Q21.1
    MCDERMID, HE
    GOODFELLOW, PJ
    DUNCAN, AMV
    BRASCH, KR
    SIMPSON, NE
    SOUZA, CD
    HOLDEN, JJA
    WHITE, BN
    NUCLEIC ACIDS RESEARCH, 1987, 15 (13) : 5498 - 5498
  • [3] A novel insertion ins(18;5)(q21.1;q31.2q35.1) in acute myeloid leukemia associated with microdeletions at 5q31.2, 5q35.1q35.2 and 18q12.3q21.1 detected by oligobased array comparative genomic hybridization
    Kjeldsen, Eigil
    MOLECULAR CYTOGENETICS, 2014, 7
  • [4] A novel insertion ins(18;5)(q21.1;q31.2q35.1) in acute myeloid leukemia associated with microdeletions at 5q31.2, 5q35.1q35.2 and 18q12.3q21.1 detected by oligobased array comparative genomic hybridization
    Eigil Kjeldsen
    Molecular Cytogenetics, 7
  • [5] Microduplication 5q11.2q21.1 presenting with congenital scoliosis
    Rengarajan, Divya
    Hara, Julia
    DuPont, Barbara
    Doherty, Emily
    GENETICS IN MEDICINE, 2022, 24 (03) : S70 - S70
  • [6] Duplication of the 1q21.1 locus leads to oligodendrocyte dysfunction
    Chapman, G. D.
    Singh, T.
    Lunn, S.
    Syed, Y. A.
    GLIA, 2019, 67 : E140 - E140
  • [7] Interstitial Deletion 5q14.3q21.3 Associated with Lethal Epilepsy
    Yang, Yong-jia
    Yao, Xu
    Guo, Jihong
    Zhao, Rui
    He, Xin-yu
    Zhao, Liu
    Tu, Ming
    Zhu, Yi-min
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (04) : 866 - 871
  • [8] PHYSICAL LOCALIZATION OF THE CHROMOSOMAL MARKER D13S31 PLACES THE WILSON DISEASE LOCUS AT THE JUNCTION OF BANDS Q14.3 AND Q21.1 OF CHROMOSOME-13
    KOOY, RF
    VANDERVEEN, AY
    VERLIND, E
    SCHEFFER, H
    BUYS, CHCM
    CYTOGENETICS AND CELL GENETICS, 1993, 62 (2-3): : 102 - 102
  • [9] ISOLATION OF NEW PROBES IN THE REGION OF THE WILSON DISEASE LOCUS, 13Q14.2-]Q14.3
    BULL, PC
    BARWELL, JA
    HANNAH, HTL
    PAUTLER, SE
    HIGGINS, MJ
    LALANDE, M
    COX, DW
    CYTOGENETICS AND CELL GENETICS, 1993, 64 (01): : 12 - 17
  • [10] A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients
    Hartmut Engels
    Eva Wohlleber
    Alexander Zink
    Juliane Hoyer
    Kerstin U Ludwig
    Felix F Brockschmidt
    Dagmar Wieczorek
    Ute Moog
    Birgit Hellmann-Mersch
    Ruthild G Weber
    Lionel Willatt
    Martina Kreiß-Nachtsheim
    Helen V Firth
    Anita Rauch
    European Journal of Human Genetics, 2009, 17 : 1592 - 1599
12345