Intracranial aneurysms in Multicase Finnish Families:: Confirmation of linkage and refinement of the interval to chromosome 19q13.3.

被引：0
|
作者：
Olson, JM
Van der Voet, M
Kuivaniemi, H
Dudek, D
Skunca, M
Ronkainen, A
Niemela, M
Jääskeläinen, J
Hernesniemi, J
Helin, K
Leinonen, E
Biswas, M
Tromp, G
机构：
[1] Case Western Reserve Univ, Cleveland, OH 44106 USA
[2] Wayne State Univ, Detroit, MI USA
[3] Univ Kuopio, FIN-70211 Kuopio, Finland
[4] Univ Helsinki, Helsinki, Finland
来源：
CIRCULATION | 2004年 / 109卷 / 07期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P13
引用
收藏
页码：E83 / E83
页数：1
相关论文
共 43 条
  • [21] LINKAGE ANALYSIS OF 19 FRENCH BREAST-CANCER FAMILIES, WITH 5 CHROMOSOME-17Q MARKERS
    MAZOYER, S
    LALLE, P
    NAROD, SA
    BIGNON, YJ
    COURJAL, F
    JAMOT, B
    DUTRILLAUX, B
    STOPPALYONNET, D
    SOBOL, H
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 52 (04) : 754 - 760
  • [22] Absence of linkage to the chromosome 4q24 Finnish migraine locus among 78 migraine families of European descent.
    Wieser, T
    Pascual, J
    Barmada, M
    Soso, M
    Oterino, A
    Gardner, K
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 480 - 480
  • [23] Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families
    Viollet, L
    Zarhrate, M
    Maystadt, I
    Estournet-Mathiaut, B
    Barois, A
    Desguerre, I
    Mayer, M
    Chabrol, B
    LeHeup, B
    Cusin, V
    de Villemeur, TB
    Bonneau, D
    Saugier-Veber, P
    Touzery-de Villepin, A
    Delaubier, A
    Kaplan, J
    Jeanpierre, M
    Feingold, J
    Munnich, A
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2004, 12 (06) : 483 - 488
  • [24] Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families
    Louis Viollet
    Mohammed Zarhrate
    Isabelle Maystadt
    Brigitte Estournet-Mathiaut
    Annie Barois
    Isabelle Desguerre
    Michèle Mayer
    Brigitte Chabrol
    Bruno LeHeup
    Veronica Cusin
    Thierry Billette de Villemeur
    Dominique Bonneau
    Pascale Saugier-Veber
    Anne Touzery-de Villepin
    Anne Delaubier
    Jocelyne Kaplan
    Marc Jeanpierre
    Joshué Feingold
    Arnold Munnich
    European Journal of Human Genetics, 2004, 12 : 483 - 488
  • [25] Twelve Single Nucleotide Polymorphisms on Chromosome 19q13.2-13.3: Linkage Disequilibria and Associations with Basal Cell Carcinoma in Danish Psoriatic Patients
    Jiaoyang Yin
    Ulla Vogel
    Lars Ulrik Gerdes
    Marianne Dybdahl
    Lars Bolund
    Bjørn Andersen Nexø
    Biochemical Genetics, 2003, 41 : 27 - 37
  • [26] Twelve single nucleotide polymorphisms on chromosome 19q13.2-13.3: Linkage disequilibria and associations with basal cell carcinoma in Danish psoriatic patients
    Yin, JY
    Vogel, U
    Gerdes, LU
    Dybdahlk, M
    Bolund, L
    Nexo, BA
    BIOCHEMICAL GENETICS, 2003, 41 (1-2) : 27 - 37
  • [27] Confirmation of linkage of the dehydrated hereditary stomatocytosis locus to chromosome 16 and refinement of the candidate region to a 6.5 cM region between 16q23-qter.
    Laurans, MSH
    Gunel, M
    Smith, BD
    Gallagher, PG
    BLOOD, 1999, 94 (10) : 190A - 190A
  • [28] Genome-wide scan of Swedish families with hereditary prostate cancer:: Suggestive evidence of linkage at 5q11.2 and 19p13.3
    Wiklund, F
    Gillanders, EM
    Albertus, JA
    Bergh, A
    Damber, JE
    Emanuelsson, M
    Freas-Lutz, DL
    Gildea, DE
    Göransson, I
    Jones, MS
    Jonsson, BA
    Lindmark, F
    Markey, CJ
    Riedesel, EL
    Stenman, E
    Trent, JM
    Grönberg, H
    PROSTATE, 2003, 57 (04): : 290 - 297
  • [29] Novel T2DM locus on chromosome 4 and confirmation of chromosome 1q21 T2DM linkage in multiplex African American families
    Elbein, SC
    Zheng, WH
    Wang, XQ
    Zhang, ZX
    Hasstedt, SJ
    DIABETES, 2004, 53 : A270 - A270
  • [30] Linkage analysis in families with Joubert syndrome plus oculo-renal involvement identifies the CORS2 locus on chromosome 11p12-q13.3
    Keeler, LC
    Marsh, SE
    Leeflang, EP
    Woods, CG
    Sztriha, L
    Al-Gazali, L
    Gururaj, A
    Gleeson, JG
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (03) : 656 - 662
12345