Eponymous Jacobsen syndrome:: Mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome

被引：6
|
作者：
Tümer, Z
Henriksen, AM
Bache, I
Larsen, LA
Tommerup, N
Brixen, K
Kalschauer, V
Illum, N
Rasmussen, K
机构：
[1] Univ Copenhagen, Fac Med, Dept Med Biochem & Geneticsm,Panum Inst, Wilhelm Johannsen Ctr Funct Genome Res, DK-2200 Copenhagen, Denmark
[2] Odense Univ Hosp, Dept Endocrinol, DK-5000 Odense, Denmark
[3] Max Planck Inst Mol Genet, Berlin, Germany
[4] Odense Univ Hosp, Dept Pediat H, DK-5000 Odense, Denmark
[5] Odense Univ Hosp, Dept Clin Biochem & Genet, DK-5000 Odense, Denmark
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2005年 / 135A卷 / 03期
关键词：
D O I：
10.1002/ajmg.a.30735
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：339 / 341
页数：3
相关论文
共 4 条
  • [1] Eponymous Jacobsen syndrome:: Mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome (vol 135, pg 339, 2006)
    Tümer, Z
    Henriksen, AM
    Bache, I
    Brixen, K
    Kalscheuer, V
    Illum, N
    Rasmussen, K
    Larsen, LA
    Tommerup, N
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (06) : 663 - 663
  • [2] Localization of Jacobsen syndrome breakpoints on a 40-Mb physical map of distal chromosome 11q
    Tunnacliffe, A
    Jones, C
    Le Paslier, D
    Todd, R
    Cherif, D
    Birdsall, M
    Devenish, L
    Yousry, C
    Cotter, FE
    James, MR
    GENOME RESEARCH, 1999, 9 (01) : 44 - 52
  • [3] Interaction Between a Chromosome 10 RET Enhancer and Chromosome 21 in the Down Syndrome-Hirschsprung Disease Association
    Arnold, Stacey
    Pelet, Anna
    Amiel, Jeanne
    Borrego, Salud
    Hofstra, Robert
    Tam, Paul
    Ceccherini, Isabella
    Lyonnet, Stanislas
    Sherman, Stephanie
    Chakravarti, Aravinda
    HUMAN MUTATION, 2009, 30 (05) : 771 - 775
  • [4] BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21
    Hubert, RS
    Mitchell, S
    Chen, XN
    Ekmekji, K
    Gadomski, C
    Sun, ZG
    Noya, D
    Kim, UJ
    Chen, CR
    Shizuya, H
    Simon, M
    deJong, PJ
    Korenberg, JR
    GENOMICS, 1997, 41 (02) : 218 - 226
1