PRENATAL EXCLUSION OF NORRIE DISEASE WITH FLANKING DNA MARKERS

被引：8

作者：

GAL, A

UHLHAAS, S

GLASER, D

GRIMM, T

机构：

[1] UNIV MUNSTER,INST HUMANGENET,D-4400 MUNSTER,FED REP GER

[2] UNIV WURZBURG,INST HUMANGENET,D-8700 WURZBURG,FED REP GER

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 31卷 / 02期

关键词：

D O I：

10.1002/ajmg.1320310225

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：449 / 453

页数：5

共 11 条

[1] CLOSE LINKAGE BETWEEN NORRIE DISEASE, A CLONED DNA-SEQUENCE FROM THE PROXIMAL SHORT ARM, AND THE CENTROMERE OF THE X-CHROMOSOME [J].

BLEEKERWAGEMAKERS, LM ;

FRIEDRICH, U ;

GAL, A ;

WIENKER, TF ;

WARBURG, M ;

ROPERS, HH .

HUMAN GENETICS, 1985, 71 (03) :211-214

[2] REPORT OF THE COMMITTEE ON THE GENETIC CONSTITUTION OF THE X-CHROMOSOMES AND Y-CHROMOSOMES [J].

DAVIES, KE ;

MANDEL, JL ;

WEISSENBACH, J ;

FELLOUS, M .

CYTOGENETICS AND CELL GENETICS, 1987, 46 (1-4) :277-315

[3]

DELACHAPELLE A, 1985, CLIN GENET, V28, P317

[4]

FORREST SM, 1987, CYTOGENET CELL GENET, V46, P615

[5]

GAL A, 1985, CYTOGENET CELL GENET, V40, P633

[6] SUBMICROSCOPIC INTERSTITIAL DELETION OF THE X-CHROMOSOME EXPLAINS A COMPLEX GENETIC SYNDROME DOMINATED BY NORRIE DISEASE [J].

GAL, A ;

WIERINGA, B ;

SMEETS, DFCM ;

BLEEKERWAGEMAKERS, L ;

ROPERS, HH .

CYTOGENETICS AND CELL GENETICS, 1986, 42 (04) :219-224

[7] X-LINKED DOMINANT CHARCOT-MARIE-TOOTH DISEASE - SUGGESTION OF LINKAGE WITH A CLONED DNA-SEQUENCE FROM THE PROXIMAL XQ [J].

GAL, A ;

MUCKE, J ;

THEILE, H ;

WIEACKER, PF ;

ROPERS, HH ;

WIENKER, TF .

HUMAN GENETICS, 1985, 70 (01) :38-42

[8] FURTHER LINKAGE DATA ON NORRIE DISEASE [J].

KIVLIN, JD ;

SANBORN, GE ;

WRIGHT, E ;

CANNON, L ;

CAREY, J .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 26 (03) :733-736

[9] PRIMARY VITREORETINAL DYSPLASIA RESEMBLING NORRIES DISEASE IN A FEMALE - ASSOCIATION WITH X-AUTOSOME CHROMOSOMAL TRANSLOCATION [J].

OHBA, N ;

YAMASHITA, T .

BRITISH JOURNAL OF OPHTHALMOLOGY, 1986, 70 (01) :64-71

[10]

WARBURG M, 1986, T OPHTHAL SOC UK, V105, P88

← 1 2 →