Characterization ofCxorf5(71-7A), a Novel Human cDNA Mapping to Xp22 and Encoding a Protein Containing Coiled-Coil α-Helical Domains

Basic local alignment search tool

1990 • 87,358 citations

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1997 • 71,835 citations

Predicting Coiled Coils from Protein Sequences

1991 • 3,977 citations

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1991 • 848 citations

Maps from two interspecific backcross DNA panels available as a community genetic mapping resource

1994 • 587 citations

Characterization of a murine gene expressed from the inactive X chromosome

1991 • 529 citations

The Human Y Chromosome: Overlapping DNA Clones Spanning the Euchromatic Region

1992 • 394 citations

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

1997 • 352 citations

Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching

1996 • 188 citations

The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: Evidence for an inversion of the Y chromosome during primate evolution

1988 • 177 citations

RI manager, a microcomputer program for analysis of data from recombinant inbred strains

1991 • 144 citations

The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3

1997 • 100 citations

A high resolution deletion map of human chromosome Xp22

1993 • 94 citations

Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts)

1996 • 87 citations

Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.

1985 • 86 citations

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3–Xp21.3

1995 • 74 citations

Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J mice

1995 • 73 citations

The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability

1995 • 64 citations

The X-Y homologous gene amelogenin maps to the short arms of both the X and Y chromosomes and is highly conserved in primates

1992 • 60 citations

Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genes

1990 • 60 citations

Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region

1996 • 57 citations

Isolation of a new gene from the distal short arm of the human X chromosome that escapes X-inactivation

1992 • 56 citations

Papel de la cartografía arterial con eco-Doppler en la toma de decisiones terapéuticas en la isquemia crítica de los miembros inferiores

2005 • 53 citations

A novel human serine-threonine phosphatase related to the Drosophila retinal degeneration C (rdgC) gene is selectively expressed in sensory neurons of neural crest origin

1997 • 52 citations

X chromosome inactivation of the human TIMP gene

1990 • 51 citations

Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes

1992 • 47 citations

Identification and isolation of transcribed human X chromosome DNA sequences

1983 • 43 citations

A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22

1996 • 42 citations

Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene?

1987 • 42 citations

Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci

1985 • 36 citations

A Novel Phenotypic Pattern in X-Linked Inheritance: Craniofrontonasal Syndrome Maps to Xp22

1997 • 35 citations

A 6-Mb YAC contig in Xp22.1–p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes

1995 • 26 citations

Genetic mapping of Xp22.12–p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL)

1995 • 22 citations

Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome

1993 • 12 citations