HUMAN FIBRONECTIN GENE (FN1) RFLPS - MAPPING AND LINKAGE DISEQUILIBRIUM ANALYSIS

被引：7
|
作者：
GARDELLA, R [1 ]
COLOMBI, M [1 ]
BARLATI, S [1 ]
机构：
[1] UNIV BRESCIA,DEPT BIOMED SCI & BIOTECHNOL,DIV BIOL & GENET,I-25123 BRESCIA,ITALY
来源：
HUMAN GENETICS | 1993年 / 92卷 / 06期
关键词：
D O I：
10.1007/BF00420958
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
We report a mapping and linkage disequilibrium analysis of six restriction fragment length polymer phisms (RFLPs) of the human fibronectin gene. The poly merase chain reaction conditions are described for four of the RFLPs.
引用
收藏
页码：639 / 641
页数：3
相关论文
共 50 条
  • [1] A TAQI RFLP FOR THE HUMAN FIBRONECTIN (FN1) GENE
    GARDELLA, R
    COLOMBI, M
    BARLATI, S
    NUCLEIC ACIDS RESEARCH, 1988, 16 (23) : 11388 - 11388
  • [2] A NEW TAQI RFLP OF THE HUMAN FIBRONECTIN (FN1) GENE
    GARDELLA, R
    COLOMBI, M
    BARLATI, S
    NUCLEIC ACIDS RESEARCH, 1989, 17 (24) : 10520 - 10520
  • [3] A FREQUENT HINDIII RFLP OF THE HUMAN FIBRONECTIN GENE (FN1)
    COLOMBI, M
    GARDELLA, R
    BARLATI, S
    NUCLEIC ACIDS RESEARCH, 1988, 16 (18) : 9074 - 9074
  • [4] A COMMON MSPI RFLP OF THE HUMAN FIBRONECTIN GENE (FN1)
    GARDELLA, R
    COLOMBI, M
    BARLATI, S
    NUCLEIC ACIDS RESEARCH, 1988, 16 (04) : 1651 - 1651
  • [5] Soft tissue tumours with FN1 (Fibronectin 1) fusion gene
    Bouvier, Corinne
    Nihous, Hugo
    Macagno, Nicolas
    ANNALES DE PATHOLOGIE, 2022, 42 (03) : 242 - 248
  • [6] Mutations in FN1 cause glomerulopathy with fibronectin deposits
    Castelletti, Federica
    Donadelli, Roberta
    Banterla, Federica
    Hildebrandt, Friedhelm
    Zipfel, Peter F.
    Bresin, Elena
    Otto, Edgar
    Skerka, Christine
    Renieri, Alessandra
    Todeschini, Marta
    Caprioli, Jessica
    Caruso, Maria Rosa
    Artuso, Rosangela
    Remuzzi, Giuseppe
    Noris, Marina
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (07) : 2538 - 2543
  • [7] A novel variant in FN1 in a family with fibronectin glomerulopathy
    Nabeel Aslam
    Anshika Singh
    Cherise Cortese
    Douglas L. Riegert-Johnson
    Human Genome Variation, 6
  • [8] A novel variant in FN1 in a family with fibronectin glomerulopathy
    Aslam, Nabeel
    Singh, Anshika
    Cortese, Cherise
    Riegert-Johnson, Douglas L.
    HUMAN GENOME VARIATION, 2019, 6 (1)
  • [9] HETEROGENEITY OF LINKAGE DISEQUILIBRIUM FOR RFLPS LINKED TO THE CF GENE IN EUROPE
    DEVOTO, M
    RONCHETTO, P
    BONDUELLE, ML
    LISSENS, W
    BALASSOPOULOU, A
    ADAM, G
    COCHAUX, P
    VASSART, G
    GEDSCHOLD, J
    BRUCKNER, R
    COUTELLE, CH
    WAINWRIGHT, B
    SEIA, M
    FERRARI, M
    CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4): : 988 - 988
  • [10] Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits
    Hiromi Ohtsubo
    Taro Okada
    Kandai Nozu
    Yutaka Takaoka
    Akemi Shono
    Katsuhiko Asanuma
    Lifang Zhang
    Koichi Nakanishi
    Mariko Taniguchi-Ikeda
    Hiroshi Kaito
    Kazumoto Iijima
    Shun-ichi Nakamura
    Pediatric Nephrology, 2016, 31 : 1459 - 1467
12345