SUBMICROSCOPIC INTERSTITIAL DELETION OF THE X-CHROMOSOME EXPLAINS A COMPLEX GENETIC SYNDROME DOMINATED BY NORRIE DISEASE

被引：71

作者：

GAL, A

WIERINGA, B

SMEETS, DFCM

BLEEKERWAGEMAKERS, L

ROPERS, HH

机构：

[1] CATHOLIC UNIV NIJMEGEN,DEPT HUMAN GENET,NIJMEGEN,NETHERLANDS

[2] NETHERLANDS OPHTHALM RES INST,DEPT OPHTHALMOGENET,AMSTERDAM,NETHERLANDS

来源：

CYTOGENETICS AND CELL GENETICS | 1986年 / 42卷 / 04期

关键词：

D O I：

10.1159/000132282

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：219 / 224

页数：6

相关论文

共 34 条

[1] BAKKER E, 1983, CLIN GENET, V23, P225
[2] BARTLEY JA, 1982, LANCET, V2, P733
[3] BLEEKERWAGEMAKE.LM, 1981, THESIS BARTIMEUS F D, P82
[4] CLOSE LINKAGE BETWEEN NORRIE DISEASE, A CLONED DNA-SEQUENCE FROM THE PROXIMAL SHORT ARM, AND THE CENTROMERE OF THE X-CHROMOSOME
BLEEKERWAGEMAKERS, LM
FRIEDRICH, U
GAL, A
WIENKER, TF
WARBURG, M
ROPERS, HH
[J]. HUMAN GENETICS, 1985, 71 (03) : 211 - 214
[5] BROEDERS GHB, 1979, NED TIJDSCHR GENEESK, V123, P1928
[6] DELACHAPELLE A, 1985, CLIN GENET, V28, P317
[7] X-LINKED HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH-HORMONE DEFICIENCY
FLEISHER, TA
WHITE, RM
BRODER, S
NISSLEY, SP
BLAESE, RM
MULVIHILL, JJ
OLIVE, G
WALDMANN, TA
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1980, 302 (26) : 1429 - 1434
[8] FRANCKE U, 1985, AM J HUM GENET, V37, P250
[9] FRANCKE U, 1984, CYTOGENET CELL GENET, V38, P298, DOI 10.1159/000132078
[10] FRIEDRICH U, 1985, 18 S EUR SOC HUM GEN

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