GENETIC-ANALYSIS OF THE FRAGILE-X MENTAL-RETARDATION SYNDROME WITH 2 FLANKING POLYMORPHIC DNA MARKERS

被引：68

作者：

OBERLE, I

HEILIG, R

MOISAN, JP

KLOEPFER, C

MATTEI, MG

MATTEI, JF

BOUE, J

FROSTERISKENIUS, U

JACOBS, PA

LATHROP, GM

LALOUEL, JM

MANDEL, JL

机构：

[1] CNRS,GENET MOLEC EUCARYOTES LAB,UNITE BIOL MOLEC & GENIE GENET 184,11,F-67085 STRASBOURG,FRANCE

[2] HOP ENFANTS TIMONE,U242,F-13385 MARSEILLE,FRANCE

[3] U73,F-75016 PARIS,FRANCE

[4] MED HSCH LUBECK,INST HUMAN GENET,D-2400 LUBECK,FED REP GER

[5] UNIV HAWAII,JOHN A BURNS SCH MED,HONOLULU,HI 96822

[6] UNIV PARIS 07,ANTHROPOL BIOL LAB,F-75221 PARIS 05,FRANCE

来源：

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | 1986年 / 83卷 / 04期

关键词：

D O I：

10.1073/pnas.83.4.1016

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

引用

页码：1016 / 1020

页数：5

共 29 条

[1] Alwine J C, 1979, Methods Enzymol, V68, P220
[2] GENETIC-LINKAGE HETEROGENEITY IN THE FRAGILE X-SYNDROME
BROWN, WT
GROSS, AC
CHAN, CB
JENKINS, EC
[J]. HUMAN GENETICS, 1985, 71 (01) : 11 - 18
[3] CLOSE LINKAGE OF FRAGILE X MENTAL-RETARDATION SYNDROME TO HEMOPHILIA-B AND TRANSMISSION THROUGH A NORMAL-MALE
CAMERINO, G
MATTEI, MG
MATTEI, JF
JAYE, M
MANDEL, JL
[J]. NATURE, 1983, 306 (5944) : 701 - 704
[4] REGIONAL LOCALIZATION ON THE HUMAN X-CHROMOSOME AND POLYMORPHISM OF THE COAGULATION FACTOR-IX GENE (HEMOPHILIA-B LOCUS)
CAMERINO, G
GRZESCHIK, KH
JAYE, M
DELASALLE, H
TOLSTOSHEV, P
LECOCQ, JP
HEILIG, R
MANDEL, JL
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (02): : 498 - 502
[5] CHOO KH, 1984, LANCET, V2, P349
[6] GENETIC-MAPPING OF THE HUMAN X-CHROMOSOME BY USING RESTRICTION FRAGMENT LENGTH POLYMORPHISMS
DRAYNA, D
DAVIES, K
HARTLEY, D
MANDEL, JL
CAMERINO, G
WILLIAMSON, R
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 DIAGNOSIS AND FREQUENCY OF X-LINKED CONDITIONS IN A COHORT OF MODERATELY RETARDED MALES WITH AFFECTED BROTHERS
FISHBURN, J
TURNER, G
DANIEL, A
BROOKWELL, R
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (04): : 713 - 724
[8] TRANSMISSION OF THE MARKER-X SYNDROME TRAIT BY UNAFFECTED MALES - CONCLUSIONS FROM STUDIES OF LARGE FAMILIES
FROSTERISKENIUS, U
SCHULZE, A
SCHWINGER, E
[J]. HUMAN GENETICS, 1984, 67 (04) : 419 - 427
[9] FRYNS JP, 1984, CLIN GENET, V26, P497
[10] CARRIER DETECTION OF HEMOPHILIA-B BY USING A RESTRICTION SITE POLYMORPHISM ASSOCIATED WITH THE COAGULATION FACTOR-IX GENE
GRUNEBAUM, L
CAZENAVE, JP
CAMERINO, G
KLOEPFER, C
MANDEL, JL
TOLSTOSHEV, P
JAYE, M
DELASALLE, H
LECOCQ, JP
[J]. JOURNAL OF CLINICAL INVESTIGATION, 1984, 73 (05) : 1491 - 1495

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