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
  • [21] A novel autosomal dominant thrombocytopenia gene maps to human chromosome 17.
    Hijioka, Y
    Fujimoto, TT
    Komatsu, K
    Yoshiura, KI
    Okita, H
    Niikawa, N
    Fujimura, K
    BLOOD, 2002, 100 (11) : 483A - 483A
  • [22] A new autosomal dominant macrothrombocytopenia maps to chromosome 9
    Morel-Kopp, P. E.
    Chen, Q.
    Liang, H. P.
    Bromhead, C.
    Britton, S.
    Turakulov, R.
    Bahlo, M.
    Stevenson, W. S.
    Ward, C. M.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2013, 11 : 284 - 284
  • [23] A novel locus for autosomal dominant congenital cerulean cataract maps to chromosome 12q
    Berry, Vanita
    Ionides, Alexander C. W.
    Moore, Anthony T.
    Bhattacharya, Shomi S.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2011, 19 (12) : 1289 - 1291
  • [24] A GENE FOR AUTOSOMAL-DOMINANT EPISODIC ATAXIA/MYOKYMIA MAPS TO CHROMOSOME-12P
    LITT, M
    KRAMER, P
    PHROMCHOTIKUL, T
    GANCHER, ST
    NUTT, JG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 1036 - 1036
  • [25] A novel locus for autosomal dominant congenital cerulean cataract maps to chromosome 12q
    Vanita Berry
    Alexander C W Ionides
    Anthony T Moore
    Shomi S Bhattacharya
    European Journal of Human Genetics, 2011, 19 : 1289 - 1291
  • [26] Autosomal Dominant Restless Legs Syndrome Maps to Chromosome 20p13 (RLS-5) in a Dutch Kindred
    Sas, Antonetta M. G.
    Di Fonzo, Alessio
    Bakker, Stef L. M.
    Simons, Erik J.
    Oostra, Ben A.
    Maat-Kievit, Anneke J.
    Boon, Agnita J. W.
    Bonifati, Vincenzo
    MOVEMENT DISORDERS, 2010, 25 (11) : 1715 - 1722
  • [27] A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly
    Schuster, H
    Toka, O
    Toka, HR
    Busjahn, A
    Öztekin, Ö
    Wienker, TF
    Bilginturan, N
    Bähring, S
    Skrabal, F
    Haller, H
    Luft, FC
    KIDNEY INTERNATIONAL, 1998, 53 (01) : 167 - 172
  • [28] A cross-over medication trial of autosomal-dominant hypertension and brachydactyly.
    Schuster, H
    Toka, O
    Toka, HR
    Busjahn, A
    Ozturk, O
    Wienker, TF
    Bilginturan, N
    Bahring, S
    Skrabal, F
    Haller, H
    Luft, FC
    HYPERTENSION, 1997, 30 (03) : P33 - P33
  • [29] Various inversions, deletions, and reinsertions on chromosome 12p in autosomal-dominant hypertension with brachydactyly -: A fish-study four families and one sporadic case
    Kann, Martin
    Baehring, Sylvia
    Kirsch, Michaela
    Rauch, Anita
    Luft, Friedrich C.
    HYPERTENSION, 2006, 48 (04) : E62 - E63
  • [30] A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15
    Morlé, L
    Bozon, M
    Zech, JC
    Alloisio, N
    Raas-Rothschild, A
    Philippe, C
    Lambert, JC
    Godet, J
    Plauchu, H
    Edery, P
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (06) : 1592 - 1597