A linkage analysis in two families with bilateral retinoblastoma

被引：0
|
作者：
Emre, S
Sungur, A
Hazar, V
Bilgic, S
Buyukpamukcu, M
Gunalp, I
机构：
来源：
TURKISH JOURNAL OF PEDIATRICS | 1996年 / 38卷 / 04期
关键词：
retinoblastoma; polymorphism; polymerase chain reaction;
D O I：
暂无
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Using polymerase chain reaction (PCR) amplification from blood samples, Xbal and BamHl polymorphisms were analyzed in two families with bilateral retinoblastoma. In one of the families it was predicted using the BamHl polymorphism that the 200 bp allele co-segregates with the disease. This family was uninformative for Xbal polymorphism. The second family was uninformative for both Xbal and BamHl polymorphism.
引用
收藏
页码：413 / 417
页数：5
相关论文
共 50 条
  • [21] Linkage analysis in families with recurrent neuroblastoma
    Perri, P
    Longo, L
    McConville, C
    Cusano, R
    Rees, SA
    Seri, M
    Conte, M
    Romeo, G
    Devoto, M
    Tonini, GP
    HORMONE-RELATED TUMORS: NOVEL APPROACHES TO PREVENTION AND TREATMENT, 2002, 963 : 74 - 84
  • [22] THE CLINICAL ANALYSIS OF 42 CASES WITH BILATERAL INTRAOCULAR RETINOBLASTOMA
    Jin, M.
    Zhao, J.
    Zhang, D.
    Yu, G.
    Wu, Q.
    Cui, Y.
    Ma, X.
    PEDIATRIC BLOOD & CANCER, 2014, 61 : S380 - S381
  • [23] RETINOBLASTOMA-GENE-ANALYSIS IN NATIVE OSTEOSARCOMA TISSUE OF A PATIENT CURED OF A BILATERAL RETINOBLASTOMA
    KABISCH, H
    SCHOLZ, RB
    WEBER, B
    HEINSOHN, S
    BUDDESTEFFEN, C
    LANDBECK, G
    KLINISCHE PADIATRIE, 1990, 202 (04): : 240 - 242
  • [24] IDENTIFICATION OF RB1 GERMLINE MUTATIONS IN ARGENTINEAN FAMILIES WITH SPORADIC BILATERAL RETINOBLASTOMA
    SZIJAN, I
    LOHMANN, DR
    PARMA, DL
    BRANDT, B
    HORSTHEMKE, B
    JOURNAL OF MEDICAL GENETICS, 1995, 32 (06) : 475 - 479
  • [25] Capturing Bilateral Retinoblastoma
    Thuma, Tobin B. T.
    Silverman, Rebecca F.
    Francis, Jasmine H.
    Abramson, David H.
    JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS, 2024,
  • [26] Linkage analysis of two families with X-linked recessive congenital motor nystagmus
    Xiangming Guo
    Shiqiang Li
    Xiaoyun Jia
    Xueshan Xiao
    Panfeng Wang
    Qingjiong Zhang
    Journal of Human Genetics, 2006, 51 : 76 - 80
  • [27] COH1 analysis and linkage study in two Japanese families with Cohen syndrome
    Kondo, I
    Shimizu, A
    Asakawa, S
    Miyamoto, K
    Yamagata, H
    Tabara, Y
    Shimizu, N
    CLINICAL GENETICS, 2005, 67 (03) : 270 - 272
  • [28] Linkage analysis of two families with X-linked recessive congenital motor nystagmus
    Guo, XM
    Li, SQ
    Jia, XY
    Xiao, XS
    Wang, PF
    Zhang, QJ
    JOURNAL OF HUMAN GENETICS, 2006, 51 (01) : 76 - 80
  • [29] APPLICATION OF POLYMORPHIC CHROMOSOME 13-SPECIFIC PROBES TO LINKAGE STUDIES IN FAMILIES WITH HEREDITARY RETINOBLASTOMA
    SCHEFFER, H
    TAN, KEWP
    BUYS, CHCM
    PEDIATRIC RESEARCH, 1986, 20 (10) : 1059 - 1059
  • [30] MUTATION ANALYSIS AND GENETIC-LINKAGE STUDIES IN RETINOBLASTOMA PATIENTS
    ONADIM, Z
    HOGG, A
    HUNGERFORD, J
    COWELL, JK
    AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 123 - 123
12345