The CEPH consortium linkage map of human chromosome 15q

Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

1980 • 8,270 citations

A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene.

1989 • 2,011 citations

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

1991 • 2,004 citations

Construction of multilocus genetic linkage maps in humans.

1987 • 1,461 citations

The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor α gene to a novel transcribed locus

1990 • 1,349 citations

A genetic linkage map of the human genome

1987 • 913 citations

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

1991 • 666 citations

Deletions of Chromosome 15 as a Cause of the Prader–Willi Syndrome

1981 • 615 citations

Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genome

1990 • 595 citations

Parameters of the human genome.

1991 • 521 citations

Location on Chromosome 15 of the Gene Defect Causing Marfan Syndrome

1990 • 380 citations

An estimate of unique DNA sequence heterozygosity in the human genome

1985 • 297 citations

Genetic Linkage of the Marfan Syndrome, Ectopia Lentis, and Congenital Contractural Arachnodactyly to the Fibrillin Genes on Chromosomes 15 and 5

1992 • 262 citations

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

1992 • 244 citations

Influence of aberrant observations on high-resolution linkage analysis outcomes.

1991 • 153 citations

A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage.

1991 • 153 citations

Systematic cloning of human minisatellites from ordered array charomid libraries

1990 • 144 citations

A mapped set of DNA markers for human chromosome 15

1988 • 130 citations

A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers

1992 • 120 citations

Tetranucleotide repeat polymorphism at the human aromatase cytochrome P-450 gene (CYP19)

1991 • 110 citations

The CEPH consortium linkage map of human chromosome 1

1991 • 96 citations

Chromosomal location of the co-expressed human skeletal and cardiac actin genes.

1984 • 76 citations

Msp-1 polymorphism detected with a cDNA probe for the P-450 I family on chromosome 15

1987 • 72 citations

The CEPH consortium primary linkage map of human chromosome 10

1990 • 69 citations

A genetic linkage map of chromosome 17

1990 • 56 citations

Dinucleotide repeat polymorphism at the D16S288 locus

1991 • 51 citations

Mapping of multiple subunits of the neuronal nicotinic acetylcholine receptor to chromosome 15 in man and chromosome 9 in mouse

1991 • 37 citations

Mapping of the thrombospondin gene to human chromosome 15 and mouse chromosome 2 by in situ hybridization

1990 • 37 citations

Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15

1992 • 35 citations

Highly polymorphic locus D15S24 (CMW-1) maps to 15pter-q13. [HGM9 provisional no. D15S24]

1988 • 34 citations

A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium study.

1992 • 23 citations

A 2-cM genetic linkage map of human chromosome 7p that includes 47 loci

1992 • 22 citations

Unbalanced reciprocal translocations in cases of Prader-Willi syndrome

1984 • 17 citations

Regional localization of the gene for cardiac muscle actin (ACTC) on chromosome 15q

1992 • 15 citations

Isolation and mapping of a polymorphic DNA sequence (pMCA1-1) on chromosome 15 [D15S33]

1988 • 10 citations

Report of the committee on the genetic constitution of chromosome 15

1991 • 8 citations

Isolation and mapping of a polymorphic DNA sequence (pEFD49.3) on chromosome 15 [Dl5S29]

1988 • 8 citations

Analysis of Genetic Linkage

2014 • 6 citations

Limb-Girdle Muscular Dystrophy is Closely Linked to the Fibrillin Locus on Chromosome 15

1993 • 6 citations

Isolation and mapping of a polymorphic DNA sequence (pEFZ33) on chromosome 15 [Dl5S45]

1988 • 5 citations

SacI and Xbal polymorphisms detected by lipocortin 2A (LPC2A)

1989 • 5 citations

Isolation and mapping of a polymorphic DNA sequence (pEFD49.2) on chromosome 15 [Dl5S38]

1988 • 3 citations

Isolation and mapping of a polymorphic DNA sequence pMCT46.2 on chromosome 15 [D15S26]

1988 • 3 citations

Isolation and mapping of a polymorphic DNA sequence (pYNM18.1) on chromosome 15 [D15S35]

1988 • 3 citations

Isolation and mapping of a polymorphic DNA sequence (pYNA15.2) on chromosome 15 [D13S36]

1988 • 2 citations

Isolation and mapping of a polymorphic DNA sequence pYNZ90.1 on chromosome 15 [D15S28]

1988 • 2 citations

Isolation and mapping of a polymorphic DNA sequence pEKZ104.1 on chromosome 15 [D15S30]

1988 • 2 citations

Isolation and mapping of a polymorphic DNA sequence (pEFD52.1) on chromosome 15 [DlSS44]

1988 • 2 citations

A new marker on chromosome 15, 1115S74, detects three RFLPs

1989 • 2 citations