Localization of the Gene for a novel syndrome characterized by Nodulosis, Arthropathy, & Osteolysis (NAO) to 16q11.2-21.

被引:0
|
作者
Kambouris, M
Meyer, BF
Mayouf, S
Sheth, K
Bahabri, S
机构
[1] King Faisal Specialist Hosp & Res Ctr, Riyadh 11211, Saudi Arabia
[2] Yale Univ, Sch Med, New Haven, CT USA
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
305
引用
收藏
页码:A59 / A59
页数:1
相关论文
共 50 条
  • [1] New form of idiopathic osteolysis: Nodulosis, arthropathy and osteolysis (NAO) syndrome
    Al-Mayouf, SM
    Majeed, M
    Hugosson, C
    Bahabri, S
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2000, 93 (01): : 5 - 10
  • [2] A novel syndrome characterized by familial arthropathy. Multicentric osteolysis and subcutaneous nodules is localized to 16q12-21.
    Al Suwairi, WM
    Al Aqeel, AI
    Gorlin, RJ
    Desnick, RJ
    Martignetti, JA
    ARTHRITIS AND RHEUMATISM, 2000, 43 (09): : S116 - S116
  • [3] A novel gene mutation for multicentric osteolysis nodulosis and arthropathy: Case report and review of literature
    Shakiba, Marjan
    Alaei, Fariba
    HELIYON, 2023, 9 (04)
  • [4] A novel mutation in the matrix metallopeptidase 2 coding gene associated with intrafamilial variability of multicentric osteolysis, nodulosis, and arthropathy
    Kroger, Liisa
    Lopponen, Tuija
    Ala-Kokko, Leena
    Kroger, Heikki
    Jauhonen, Hanna-Mari
    Lehti, Kaisa
    Jaaskelainen, Jarmo
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (08):
  • [5] POSSIBLE MAPPING OF THE GENE FOR TRANSIENT MYELOPROLIFERATIVE SYNDROME AT 21Q11.2
    NIIKAWA, N
    DENG, HX
    ABE, K
    HARADA, N
    OKADA, T
    TSUCHIYA, H
    AKABOSHI, I
    MATSUDA, I
    FUKUSHIMA, Y
    KANEKO, Y
    KUWANO, A
    KAJII, T
    HUMAN GENETICS, 1991, 87 (05) : 561 - 566
  • [6] Al-Aqeel Sewairi syndrome, a new autosomal recessive disorder with multicentric osteolysis, nodulosis and arthropathy - The first genetic defect of matrix metalloproteinase 2 gene
    Al-Aqeel, AL
    SAUDI MEDICAL JOURNAL, 2005, 26 (01) : 24 - 30
  • [7] POSSIBLE MAPPING OF THE GENE RESPONSIBLE FOR TRANSIENT MYELOPROLIFERATIVE SYNDROME (TMS) AT 21Q11.2
    NIIKAWA, N
    ABE, K
    DENG, HX
    FUKUSHIMA, Y
    KAJII, T
    AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 246 - 246
  • [8] Novel chromosome 16 abnormality-der(16)del(16) (q13)t(16;21)(p11.2;q22)-associated with acute myeloid leukemia
    Sharma, P
    Watson, N
    Robson, L
    Gallo, J
    Smith, A
    CANCER GENETICS AND CYTOGENETICS, 1999, 113 (01) : 25 - 28
  • [9] Computational analysis of missense variants in MMP2 gene linked with Winchester syndrome and Nodulosis-Arthropathy-Osteolysis reveals structural shift in protein-protein and protein-ligand complexes
    Rangasamy, Nithya
    Kumar, Nachimuthu Senthil
    Santhy, K. S.
    META GENE, 2021, 29
  • [10] Localization of a multiple synostoses syndrome disease gene to chromosome 17q21-22
    Krakow, D
    Reinker, K
    Powell, B
    Cantor, R
    Priore, MA
    Garber, A
    Lachman, RS
    Rimoin, DL
    Cohn, DH
    AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) : 120 - 124