REPORT OF THE 2ND INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-15 MAPPING 1994

被引：18

作者：

MALCOLM, S ^{[1
]}

DONLON, TA ^{[1
]}

机构：

[1] KAPIOLANI MED CTR,HONOLULU,HI

来源：

CYTOGENETICS AND CELL GENETICS | 1994年 / 67卷 / 01期

关键词：

D O I：

10.1159/000133717

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

[No abstract available]

引用

页码：1 / 14

页数：14

共 17 条

[1]

ALBERTSEN HM, 1990, P NATL ACAD SCI USA, V87, P1213

[2] A LINKAGE MAP OF HUMAN-CHROMOSOME-15 WITH AN AVERAGE RESOLUTION OF 2 CM AND CONTAINING 55 POLYMORPHIC MICROSATELLITES [J].

BECKMANN, JS ;

TOMFOHRDE, J ;

BARNES, RI ;

WILLIAMS, M ;

BROUX, O ;

RICHARD, I ;

WEISSENBACH, J ;

BOWCOCK, AM .

HUMAN MOLECULAR GENETICS, 1993, 2 (12) :2019-2030

[3] CLONING OF LARGE SEGMENTS OF EXOGENOUS DNA INTO YEAST BY MEANS OF ARTIFICIAL CHROMOSOME VECTORS [J].

BURKE, DT ;

CARLE, GF ;

OLSON, MV .

SCIENCE, 1987, 236 (4803) :806-812

[4]

DESOUZA AP, 1994, IN PRESS GENOMICS, V19

[5] MAPPING OF A CHROMOSOME-15 REGION INVOLVED IN LIMB-GIRDLE MUSCULAR-DYSTROPHY [J].

FOUGEROUSSE, F ;

BROUX, O ;

RICHARD, I ;

ALLAMAND, V ;

DESOUZA, AP ;

BOURG, N ;

BRENGUIER, L ;

DEVAUD, C ;

PASTURAUD, P ;

ROUDAUT, C ;

CHIANNILKULCHAI, N ;

HILLAIRE, D ;

BUI, H ;

CHUMAKOV, I ;

WEISSENBACH, J ;

CHERIF, D ;

COHEN, D ;

BECKMANN, JS .

HUMAN MOLECULAR GENETICS, 1994, 3 (02) :285-293

[6] MUTATIONS IN THE FIBRILLIN GENE RESPONSIBLE FOR DOMINANT ECTOPIA LENTIS AND NEONATAL MARFAN-SYNDROME [J].

KAINULAINEN, K ;

KARTTUNEN, L ;

PUHAKKA, L ;

SAKAI, L ;

PELTONEN, L .

NATURE GENETICS, 1994, 6 (01) :64-69

[7] ALLELE SPECIFICITY OF DNA-REPLICATION TIMING IN THE ANGELMAN PRADER-WILLI-SYNDROME IMPRINTED CHROMOSOMAL REGION [J].

KNOLL, JHM ;

CHENG, SD ;

LALANDE, M .

NATURE GENETICS, 1994, 6 (01) :41-46

[8] MUTATIONS OF THE P-GENE IN OCULOCUTANEOUS ALBINISM, OCULAR ALBINISM, AND PRADER-WILLI-SYNDROME PLUS ALBINISM [J].

LEE, ST ;

NICHOLLS, RD ;

BUNDEY, S ;

LAXOVA, R ;

MUSARELLA, M ;

SPRITZ, RA .

NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (08) :529-534

[9] A NOVEL MUTATION OF THE FIBRILLIN GENE CAUSING ECTOPIA LENTIS [J].

LONNQVIST, L ;

CHILD, A ;

KAINULAINEN, K ;

DAVIDSON, R ;

PUHAKKA, L ;

PELTONEN, L .

GENOMICS, 1994, 19 (03) :573-576

[10] A CENTROMERE MAP OF THE X-CHROMOSOME FROM TRISOMIES OF MATERNAL ORIGIN [J].

MORTON, NE ;

KEATS, BJ ;

JACOBS, PA ;

HASSOLD, T ;

PETTAY, D ;

HARVEY, J ;

ANDREWS, V .

ANNALS OF HUMAN GENETICS, 1990, 54 :39-47

← 1 2 →