Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12

被引:113
|
作者
Schuster, H
Wienker, TF
Bahring, S
Bilginturan, N
Toka, HR
Neitzel, H
Jeschke, E
Toka, O
Gilbert, D
Lowe, A
Ott, J
Haller, H
Luft, FC
机构
[1] HUMBOLDT UNIV BERLIN,UNIV HOSP RUDOLF VIRCHOW,MAX DELBRUCK CTR MOLEC MED,FRANZ VOLHARD CLIN,BERLIN,GERMANY
[2] HACETTEPE UNIV,SCH MED,DEPT PEDIAT,SECT PEDIAT ENDOCRINOL,ANKARA,TURKEY
关键词
D O I
10.1038/ng0596-98
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:98 / 100
页数:3
相关论文
共 50 条
  • [31] CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY MAPS TO CHROMOSOME-19Q12
    TOURNIERLASSERVE, E
    JOUTEL, A
    MELKI, J
    WEISSENBACH, J
    LATHROP, GM
    CHABRIAT, H
    MAS, JL
    CABANIS, EA
    BAUDRIMONT, M
    MACIAZEK, J
    BACH, MA
    BOUSSER, MG
    NATURE GENETICS, 1993, 3 (03) : 256 - 259
  • [32] CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS MAPS TO CHROMOSOME-19Q12
    TOURNIERLASSERVE, E
    JOUTEL, A
    MELKI, J
    WEISSENBACH, J
    LATHROP, GM
    CHABRIAT, H
    MAS, JL
    NIBBIO, A
    CABANIS, EA
    BAUDRIMONT, M
    MACIAZEK, J
    BACH, MA
    BOUSSER, MG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 1091 - 1091
  • [33] Complex rearrangements cause hypertension and brachydactyly on the short arm of chromosome 12
    Bähring, S
    Rauch, A
    Aydin, A
    Toka, O
    Toka, HR
    Jordan, J
    Reis, A
    Luft, FC
    HYPERTENSION, 2003, 42 (03) : 443 - 443
  • [34] Hypertension and brachydactyly on the short arm of chromosome 12 are caused by complex rearrangements
    Bähring, S
    Rauch, A
    Aydin, A
    Toka, O
    Jordan, J
    Toka, HR
    Reis, A
    Luft, FC
    HYPERTENSION, 2003, 42 (04) : 629 - 629
  • [35] Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish family
    Bahring, S
    Nagai, T
    Toka, HR
    Nitz, I
    Toka, O
    Aydin, A
    Muhl, A
    Wienker, TF
    Schuster, H
    Luft, FC
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 60 (03) : 732 - 735
  • [36] A new locus for autosomal dominant congenital cataracts maps to chromosome 3
    Kramer, PL
    LaMorticella, D
    Schilling, K
    Billingslea, AM
    Weleber, RG
    Litt, M
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (01) : 36 - 39
  • [37] A unique, autosomal dominant, bone and dental dysplasia in a 4-generation American kindred.
    Wenkert, D.
    McAlister, W. H.
    Novack, D. V.
    Sedighi, H.
    Horwith, M.
    Whyte, M. P.
    JOURNAL OF BONE AND MINERAL RESEARCH, 2006, 21 : S430 - S430
  • [38] A LARGE NEW-ENGLAND KINDRED WITH AUTOSOMAL DOMINANT NEUROGENIC SCAPULOPERONEAL AMYOTROPHY WITH UNIQUE FEATURES
    DELONG, R
    SIDDIQUE, T
    ARCHIVES OF NEUROLOGY, 1992, 49 (09) : 905 - 908
  • [39] A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11p12-13
    Downey, LM
    Keen, TJ
    Roberts, E
    Mansfield, DC
    Bamashmus, M
    Inglehearn, CF
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (03) : 778 - 781
  • [40] A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13
    Brancati, F
    Valente, EM
    Sarkozy, A
    Fehèr, J
    Castori, M
    Del Duca, P
    Mingarelli, R
    Pizzuti, A
    Dallapiccola, B
    JOURNAL OF MEDICAL GENETICS, 2004, 41 (03) : 188 - 192