A NEW DNA PROBE PROXIMAL TO AND CLOSELY LINKED TO FRAGILE-X

被引：4

作者：

CARPENTER, NJ ^{[1
]}

VEENEMA, H ^{[1
]}

BAKKER, E ^{[1
]}

HOFKER, MH ^{[1
]}

PEARSON, PL ^{[1
]}

机构：

[1] UNIV LEIDEN,SYLVIUS LAB,DEPT HUMAN GENET,LEIDEN,NETHERLANDS

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 27卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320270332

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：731 / 732

页数：2

共 10 条

[1] DNA LINKAGE STUDIES IN THE FRAGILE-X SYNDROME SUGGEST GENETIC-HETEROGENEITY [J].

BROWN, WT ;

GROSS, AC ;

CHAN, CB ;

JENKINS, EC .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2) :643-664

[2] AN ASSESSMENT OF THE USE OF FLANKING DNA MARKERS FOR FRA(X) SYNDROME CARRIER DETECTION AND PRENATAL-DIAGNOSIS [J].

FORSTERGIBSON, CJ ;

MULLIGAN, LM ;

SIMPSON, NE ;

WHITE, BN ;

HOLDEN, JJA .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2) :665-683

[3]

HOFKER MH, 1985, HUM GENE MAPPING, V8, P652

[4]

LATHROP GM, 1984, AM J HUM GENET, V36, P460

[5] LOCALIZATION BY INSITU HYBRIDIZATION OF THE COAGULATION FACTOR-IX GENE AND OF 2 POLYMORPHIC DNA PROBES WITH RESPECT TO THE FRAGILE-X SITE [J].

MATTEI, MG ;

BAETEMAN, MA ;

HEILIG, R ;

OBERLE, I ;

DAVIES, K ;

MANDEL, JL ;

MATTEI, JF .

HUMAN GENETICS, 1985, 69 (04) :327-331

[6] GENETIC-ANALYSIS OF THE FRAGILE-X MENTAL-RETARDATION SYNDROME WITH 2 FLANKING POLYMORPHIC DNA MARKERS [J].

OBERLE, I ;

HEILIG, R ;

MOISAN, JP ;

KLOEPFER, C ;

MATTEI, MG ;

MATTEI, JF ;

BOUE, J ;

FROSTERISKENIUS, U ;

JACOBS, PA ;

LATHROP, GM ;

LALOUEL, JM ;

MANDEL, JL .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (04) :1016-1020

[7] FURTHER SEGREGATION ANALYSIS OF THE FRAGILE-X SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES [J].

SHERMAN, SL ;

JACOBS, PA ;

MORTON, NE ;

FROSTERISKENIUS, U ;

HOWARDPEEBLES, PN ;

NIELSEN, KB ;

PARTINGTON, MW ;

SUTHERLAND, GR ;

TURNER, G ;

WATSON, M .

HUMAN GENETICS, 1985, 69 (04) :289-299

[8] THE MARKER (X) SYNDROME - A CYTOGENETIC AND GENETIC-ANALYSIS [J].

SHERMAN, SL ;

MORTON, NE ;

JACOBS, PA ;

TURNER, G .

ANNALS OF HUMAN GENETICS, 1984, 48 (JAN) :21-37

[9] CYTOLOGICAL MAPPING OF THE HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE DISTAL TO THE FRAGILE-X SITE SUGGESTS A HIGH-RATE OF MEIOTIC RECOMBINATION ACROSS THIS SITE [J].

SZABO, P ;

PURRELLO, M ;

ROCCHI, M ;

ARCHIDIACONO, N ;

ALHADEFF, B ;

FILIPPI, G ;

TONIOLO, D ;

MARTINI, G ;

LUZZATTO, L ;

SINISCALCO, M .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (24) :7855-7859

[10] THE FRAGILE X-SYNDROME IN A LARGE FAMILY .1. CYTOGENETIC AND CLINICAL INVESTIGATIONS [J].

VEENEMA, H ;

GERAEDTS, JPM ;

BEVERSTOCK, GC ;

PEARSON, PL .

JOURNAL OF MEDICAL GENETICS, 1987, 24 (01) :23-31

← 1 →