DNA LINKAGE STUDIES IN THE FRAGILE-X SYNDROME SUGGEST GENETIC-HETEROGENEITY

被引：49

作者：

BROWN, WT

GROSS, AC

CHAN, CB

JENKINS, EC

机构：

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1986年 / 23卷 / 1-2期

关键词：

D O I：

10.1002/ajmg.1320230158

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：643 / 664

页数：22

共 15 条

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MATTEI, MG
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MANDEL, JL
[J]. NATURE, 1983, 306 (5944) : 701 - 704
[3] CHOO KH, 1984, LANCET, V2, P349
[4] DAVIES KE, 1985, HUM GENET, V70, P249
[5] CLONING OF A REPRESENTATIVE GENOMIC LIBRARY OF THE HUMAN X-CHROMOSOME AFTER SORTING BY FLOW-CYTOMETRY
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YOUNG, BD
ELLES, RG
HILL, ME
WILLIAMSON, R
[J]. NATURE, 1981, 293 (5831) : 374 - 376
[6] GENETIC-MAPPING OF THE HUMAN X-CHROMOSOME BY USING RESTRICTION FRAGMENT LENGTH POLYMORPHISMS
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MANDEL, JL
CAMERINO, G
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WHITE, R
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (09): : 2836 - 2839
[7] THE GENETIC-DISTANCE BETWEEN THE COAGULATION FACTOR-IX GENE AND THE LOCUS FOR THE FRAGILE-X SYNDROME - CLINICAL IMPLICATIONS
FORSTERGIBSON, CJ
MULLIGAN, LM
PARTINGTON, MW
SIMPSON, NE
HOLDEN, JJA
WHITE, BN
[J]. JOURNAL OF NEUROGENETICS, 1985, 2 (03) : 231 - 237
[8] GARDNER RJM, 1983, CLIN GENET, V23, P311
[9] HODGE SE, 1983, AM J HUM GENET, V35, P1319
[10] ISOLATION AND CHARACTERIZATION OF A CDNA CODING FOR HUMAN FACTOR-IX
KURACHI, K
DAVIE, EW
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (21): : 6461 - 6464