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
  • [41] Unique evidence for autosomal dominant inheritance of severe congenital neutropenia.
    Boxer, LA
    Stein, S
    Buckley, D
    Subramanian, S
    Bolyard, AA
    Olson, MV
    Dale, DC
    BLOOD, 2004, 104 (11) : 408A - 408A
  • [42] A family with autosomal dominant dilated cardiomyopathy maps to a novel locus in chromosome 2
    Jung, M
    Poepping, I
    Parrot, A
    Ellmer, AE
    Reis, A
    Osterziel, KJ
    CIRCULATION, 1998, 98 (17) : 246 - 246
  • [43] Autosomal dominant restless legs syndrome maps on chromosome 14q
    Bonati, MT
    Ferini-Strambi, L
    Aridon, P
    Oldani, A
    Zucconi, M
    Casari, G
    BRAIN, 2003, 126 : 1485 - 1492
  • [44] Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q
    DeStefano, AL
    Baldwin, CT
    Burzstyn, M
    Gavras, I
    Handy, DE
    Joost, O
    Martel, T
    Nicolaou, M
    Schwartz, F
    Streeten, DHP
    Farrer, LA
    Gavras, H
    AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (05) : 1425 - 1430
  • [45] AUTOSOMAL-DOMINANT CONE DEGENERATION MAPS TO CHROMOSOME 17P
    SMALL, KW
    MULLEN, L
    SYRQUIN, M
    GEHRS, K
    INANA, G
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 1171 - 1171
  • [46] Autosomal dominant moyamoya disease maps to chromosome 17q25.3
    Mineharu, Y.
    Liu, W.
    Inoue, K.
    Matsuura, N.
    Inoue, S.
    Takenaka, K.
    Ikeda, H.
    Houkin, K.
    Takagi, Y.
    Kikuta, K.
    Nozaki, K.
    Hashimoto, N.
    Koizumi, A.
    NEUROLOGY, 2008, 70 (24) : 2357 - 2363
  • [47] A new locus on chromosome 12p13.3 for pseudohypoaldosteronism type II, autosomal dominant form of hypertension
    Disse-Nicodème, S
    Achard, JM
    Desitter, I
    Houot, AM
    Fournier, A
    Corvol, P
    Jeunemaitre, X
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (02) : 302 - 310
  • [48] A new locus on chromosome 12p13.3 for pseudohypoaldosteronism type II, an autosomal dominant form of hypertension
    Disse-Nicodème, S
    Achard, JM
    Desitter, I
    Houot, AM
    Fourmier, A
    Corvol, P
    Jeunemaitre, X
    HYPERTENSION, 2000, 36 (04) : 657 - 657
  • [49] Liddle syndrome: An autosomal dominant form of human hypertension
    Warnock, DG
    KIDNEY INTERNATIONAL, 1998, 53 (01) : 18 - 24
  • [50] A novel form of autosomal dominant pure spastic paraplegia (SP) maps to chromosome 12q23-24
    Schule, Rebecca
    Durr, Alexandra
    Kassubek, Jan
    Klimpe, Sven
    Van De Warrenburg, B. P. C.
    Schoels, Ludger
    NEUROLOGY, 2007, 68 (12) : A252 - A252