INTEGRITY OF THE THYROGLOBULIN LOCUS IN TRICHORHINOPHALANGEAL SYNDROME-II

被引：14

作者：

BROCAS, H

BUHLER, EM

SIMON, P

MALIK, NJ

VASSART, G

机构：

[1] UNIV LIBRE BRUXELLES,FAC MED,INST RECH INTERDISCIPLINAIRE,CAMPUS ERASME,ROUTE LENNIK 808,B-1070 BRUSSELS,BELGIUM

[2] UNIV BASEL,INST GENET,KINDER KLIN,CH-4005 BASEL,SWITZERLAND

[3] UNIV LIBRE BRUXELLES,FAC MED,SERV CHIM CLIN,B-1070 BRUSSELS,BELGIUM

来源：

HUMAN GENETICS | 1986年 / 74卷 / 02期

关键词：

D O I：

10.1007/BF00282087

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：178 / 180

页数：3

共 17 条

[1] MAPPING OF HUMAN THYROGLOBULIN GENE ON THE LONG ARM OF CHROMOSOME-8 BY INSITU HYBRIDIZATION [J].

AVVEDIMENTO, VE ;

DILAURO, R ;

MONTICELLI, A ;

BERNARDI, F ;

PATRACCHINI, P ;

CALZOLARI, E ;

MARTINI, G ;

VARRONE, S .

HUMAN GENETICS, 1985, 71 (02) :163-166

[2] UNUSUAL SCARCITY OF RESTRICTION SITE POLYMORPHISM IN THE HUMAN THYROGLOBULIN GENE - A LINKAGE STUDY SUGGESTING AUTOSOMAL DOMINANCE OF A DEFECTIVE THYROGLOBULIN ALLELE [J].

BAAS, F ;

BIKKER, H ;

VANOMMEN, GJB ;

DEVIJLDER, JJM .

HUMAN GENETICS, 1984, 67 (03) :301-305

[3] THE HUMAN THYROGLOBULIN GENE - A POLYMORPHIC MARKER LOCALIZED DISTAL TO C-MYC ON CHROMOSOME-8 BAND-Q24 [J].

BAAS, F ;

BIKKER, H ;

VANKESSEL, AG ;

MELSERT, R ;

PEARSON, PL ;

DEVIJLDER, JJM ;

VANOMMEN, GJB .

HUMAN GENETICS, 1985, 69 (02) :138-143

[4] LOCALIZATION OF THE THYROGLOBULIN GENE BY INSITU HYBRIDIZATION TO HUMAN-CHROMOSOMES [J].

BERGELEFRANC, JL ;

CARTOUZOU, G ;

MATTEI, MG ;

PASSAGE, E ;

MALEZETDESMOULINS, C ;

LISSITZKY, S .

HUMAN GENETICS, 1985, 69 (01) :28-31

[5]

BOWEN P, 1985, ANN GENET-PARIS, V28, P224

[6] CLONING OF HUMAN THYROGLOBULIN COMPLEMENTARY-DNA [J].

BROCAS, H ;

CHRISTOPHE, D ;

POHL, V ;

VASSART, G .

FEBS LETTERS, 1982, 137 (02) :189-192

[7] CHROMOSOME DELETION AND MULTIPLE CARTILAGINOUS EXOSTOSES [J].

BUHLER, EM ;

BUHLER, UK ;

STALDER, GR ;

JANI, L ;

JURIK, LP .

EUROPEAN JOURNAL OF PEDIATRICS, 1980, 133 (02) :163-166

[8] THE TRICHO-RHINO-PHALANGEAL SYNDROME(S) - CHROMOSOME-8 LONG ARM DELETION - IS THERE A SHORTEST REGION OF OVERLAP BETWEEN REPORTED CASES - TRP-I AND TRP-II SYNDROMES - ARE THEY SEPARATE ENTITIES [J].

BUHLER, EM ;

MALIK, NJ .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 19 (01) :113-119

[9] TERMINAL OR INTERSTITIAL DELETION IN CHROMOSOME-8 LONG ARM IN LANGER-GIEDION SYNDROME (TRP-II SYNDROME) [J].

BUHLER, EM ;

BUHLER, UK ;

CHRISTEN, R .

HUMAN GENETICS, 1983, 64 (02) :163-166

[10] LANGER-GIEDION SYNDROME AND DELETION OF THE LONG ARM OF CHROMOSOME-8 - CONFIRMATION OF THE CRITICAL SEGMENT TO 8Q23 [J].

FRYNS, JP ;

HEREMANS, G ;

MARIEN, J ;

VANDENBERGHE, H .

HUMAN GENETICS, 1983, 64 (02) :194-195

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