Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma

被引：100
作者：
Bausch, Birke [1 ]
Borozdin, Wiktor [1 ]
Neumann, Hartmut P. H. [1 ]
机构：
[1] Univ Freiburg, D-79106 Freiburg, Germany
来源：
NEW ENGLAND JOURNAL OF MEDICINE | 2006年 / 354卷 / 25期
关键词：
MECHANISM;
D O I：
10.1056/NEJMc066006
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：2729 / 2731
页数：3
相关论文
共 6 条
  • [1] SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism -: art. no. e113
    Borozdin, W
    Boehm, D
    Leipoldt, M
    Wilhelm, C
    Reardon, W
    Clayton-Smith, J
    Becker, K
    Mühlendyck, H
    Winter, R
    Giray, Ö
    Silan, F
    Kohlhase, J
    [J]. JOURNAL OF MEDICAL GENETICS, 2004, 41 (09) : e113
  • [2] Pheochromocytoma - Death of an axiom.
    Dluhy, RG
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (19) : 1486 - 1488
  • [3] Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22
    Luijten, M
    Wang, YP
    Smith, BT
    Westerveld, A
    Smink, LJ
    Dunham, I
    Roe, BA
    Hulsebos, TJM
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2000, 8 (03) : 209 - 214
  • [4] Neumann HPH, 2004, JAMA-J AM MED ASSOC, V292, P1686, DOI 10.1001/jama.292.8.943
  • [5] Neumann HPH, 2004, JAMA-J AM MED ASSOC, V292, P943, DOI 10.1001/jama.292.8.943
  • [6] VONRECKLINGHAUSEN NEUROFIBROMATOSIS
    RICCARDI, VM
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1981, 305 (27) : 1617 - 1627
1