Genetic and physical mapping around the properdin P gene

Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia

1985 • 9,128 citations

Strategies for multilocus linkage analysis in humans.

1984 • 2,600 citations

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

1990 • 595 citations

Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction.

1990 • 454 citations

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

1984 • 296 citations

The alternative pathway of complement

1984 • 294 citations

Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests.

1990 • 233 citations

Chromosome maps of man and mouse. IV

1989 • 219 citations

Revision of consensus sequence of human Alu repeats — a review

1987 • 203 citations

Five polymorphic microsatellite VNTRs on the human X chromosome.

1990 • 164 citations

Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries.

1991 • 160 citations

Dinucleotide repeat polymorphism at the MAOA locus

1991 • 124 citations

Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: Implications for norrie disease

1989 • 122 citations

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease

1986 • 75 citations

Multi-allelic RFLP for M27β, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255]

1987 • 69 citations

Norrie disease resulting from a gene deletion: clinical features and DNA studies.

1988 • 69 citations

Interaction of complement with Neisseria meningitidis and Neisseria gonorrhoeae

1989 • 67 citations

Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3

1989 • 64 citations

Molecular cloning of the cDNA coding for properdin, a positive regulator of the alternative pathway of human complement

1991 • 62 citations

Physical mapping of 60 DNA markers in the p21.1 → q21.3 region of the human X chromosome

1991 • 61 citations

Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22–Xp11.3

1991 • 60 citations

A cytological map of the human X chromosome - evidence for non-random recombination

1984 • 48 citations

Localization of the properdin structural locus to Xp11.23–Xp21.1

1989 • 47 citations

Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa.

1990 • 41 citations

Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.

1985 • 38 citations

An 18-locus linkage map of the pericentromeric region of the human X chromosome: Genetic framework for mapping X-linked disorders

1991 • 36 citations

Linkage analysis of the properdin deficiency gene: Suggestion of a locus in the proximal part of the short arm of the X chromosome

1988 • 23 citations

Pairwise linkage analysis of 11 loci on human chromosome 4.

1988 • 17 citations

The properdin structural locus (Pfc) lies close to the locus for tissue inhibitor of metallothionine proteases (Timp) on the mouse X chromosome

1991 • 11 citations

Non‐allelic mutations in X‐linked retinitis pigmentosa

1989 • 10 citations