Regional localisation of a non‐specific X‐linked mental retardation gene (MRX19) to Xp22

急性心筋梗塞の疑いのある17187症例におけるストレプトキナーゼ静脈内投与,アスピリン経口投与,上記2つの併用または無処置の無作偽試験 ISIS-2

1988 • 2,760 citations

A second-generation linkage map of the human genome

1992 • 1,721 citations

DNA typing and genetic mapping with trimeric and tetrameric tandem repeats.

1991 • 1,170 citations

Report of the committee on methods of linkage analysis and reporting

1985 • 325 citations

Fragile sites on human chromosomes

1985 • 316 citations

Nonspecific X‐linked mental retardation II: The frequency in British Columbia

1980 • 272 citations

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.

1989 • 256 citations

Fragile Sites on Human Chromosomes

1986 • 242 citations

Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses

1992 • 168 citations

Five polymorphic microsatellite VNTRs on the human X chromosome.

1990 • 164 citations

Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene.

1991 • 140 citations

Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes

1993 • 130 citations

Report of the committee on linkage and gene order

1988 • 119 citations

A high resolution deletion map of human chromosome Xp22

1993 • 94 citations

Report of the committee on linkage and gene order

1989 • 76 citations

Non-specific X linked mental retardation.

1991 • 70 citations

Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci

1990 • 58 citations

Nomenclature guidelines for X‐linked mental retardation

1992 • 58 citations

Linkage analysis suggests at least two loci for X‐linked nonspecific mental retardation

1988 • 54 citations

Genetic and physical mapping around the properdin P gene

1991 • 46 citations

Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.

1991 • 45 citations

An informative polymorphism detectable by polymerase chain reaction at the 3? end of the dystrophin gene

1990 • 45 citations

Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3.

1993 • 44 citations

A Linkage Map of Microsatellite Markers on the Human X Chromosome

1994 • 34 citations

XLMR genes: Update 1992

1992 • 32 citations

A study of mental retardation in children in the Island of Hawaii

1983 • 28 citations

Report of the Fourth International Workshop on Human X Chromosome Mapping 1993 (Part 1 of 4)

1993 • 27 citations

Non‐specific X‐linked mental retardation: Linkage analysis in MRX2 and MRX4 families revisited

1994 • 27 citations

Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease gene.

1993 • 26 citations

A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3)

1991 • 26 citations

X‐linked mental retardation with dystonic movements of the hands (PRTS): Revisited

1994 • 22 citations

Characterization of new PCR based markers for mapping and diagnosis: AC dinucleotide repeat markers at the DXS237 (GMGX9) and DXS102 (cX38.1) loci

1992 • 22 citations

Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci

1992 • 20 citations

Integration of the cytogenetic and genetic linkage maps of human chromosome 16 using 50 physical intervals and 50 polymorphic loci

1993 • 11 citations