ASSIGNMENT OF THE PEPSINOGEN GENE-COMPLEX (PGA) TO HUMAN-CHROMOSOME REGION 11Q13 BY INSITU HYBRIDIZATION

被引:49
作者
NAKAI, H
BYERS, MG
SHOWS, TB
TAGGART, RT
机构
[1] NEW YORK STATE DEPT HLTH,ROSWELL PK MEM INST,DEPT HUMAN GENET,666 ELM ST,BUFFALO,NY 14263
[2] VET ADM MED CTR,SEPULVEDA,CA 91343
[3] UNIV CALIF LOS ANGELES,SCH MED,DEPT MED,LOS ANGELES,CA 90024
来源
CYTOGENETICS AND CELL GENETICS | 1986年 / 43卷 / 3-4期
关键词
D O I
10.1159/000132324
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
引用
收藏
页码:215 / 217
页数:3
相关论文
共 10 条
  • [1] REPORT OF THE COMMITTEE ON CHROMOSOME REARRANGEMENTS IN NEOPLASIA AND ON FRAGILE SITES
    BERGER, R
    BLOOMFIELD, CD
    SUTHERLAND, GR
    [J]. CYTOGENETICS AND CELL GENETICS, 1985, 40 (1-4): : 490 - 535
  • [2] REPORT OF THE COMMITTEE ON THE GENETIC CONSTITUTION OF CHROMOSOMES-10, CHROMOSOMES-11 AND CHROMOSOMES-12
    GRZESCHIK, KH
    KAZAZIAN, HH
    [J]. CYTOGENETICS AND CELL GENETICS, 1985, 40 (1-4): : 179 - 205
  • [3] SAMLOFF IM, 1982, GASTROENTEROLOGY, V82, P26
  • [4] SOGAWA K, 1983, J BIOL CHEM, V258, P5306
  • [5] VARIABLE NUMBERS OF PEPSINOGEN GENES ARE LOCATED IN THE CENTROMERIC REGION OF HUMAN CHROMOSOME-11 AND DETERMINE THE HIGH-FREQUENCY ELECTROPHORETIC POLYMORPHISM
    TAGGART, RT
    MOHANDAS, TK
    SHOWS, TB
    BELL, GI
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (18) : 6240 - 6244
  • [6] TAGGART RT, 1986, IN PRESS J HUM GENET
  • [7] HIGH-RESOLUTION CHROMOSOMAL LOCALIZATION OF HUMAN GENES FOR AMYLASE, PROOPIOMELANOCORTIN, SOMATOSTATIN, AND A DNA FRAGMENT (D3S1) BY INSITU HYBRIDIZATION
    ZABEL, BU
    NAYLOR, SL
    SAKAGUCHI, AY
    BELL, GI
    SHOWS, TB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (22): : 6932 - 6936
  • [8] ASSIGNMENT OF HUMAN PEPSINOGEN-A LOCUS TO THE Q12-PTER REGION OF CHROMOSOME-11
    ZELLE, B
    VANKESSEL, AG
    DEWIT, J
    EVERS, P
    ARWERT, F
    PRONK, JC
    MAGER, WH
    PLANTA, RJ
    ERIKSSON, AW
    FRANTS, RR
    [J]. HUMAN GENETICS, 1985, 70 (04) : 337 - 340
  • [9] 1981, BIRTH DEFECTS ORIGIN, V17, P1
  • [10] 1981, CYTOGENET CELL GENET, V31, P1