Mapping of the X linked form of hyper IgM syndrome (HIGM1)

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

1991 • 1,170 citations

Molecular and biological characterization of a murine ligand for CD40

1992 • 1,029 citations

Mendelian Inheritance in Man

1987 • 599 citations

A strategy to reveal high-frequency RFLPs along the human X chromosome.

1984 • 361 citations

A rapid method for the purification of DNA from blood

1987 • 323 citations

Immunodeficiency with hyper-IgM (HIM).

1992 • 318 citations

Anti-CD40 monoclonal antibodies or CD4+ T cell clones and IL-4 induce IgG4 and IgE switching in purified human B cells via different signaling pathways.

1991 • 270 citations

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 622-643

1989 • 212 citations

RECURRENT BACTERIAL INFECTIONS AND DYSGAMMAGLOBULINEMIA: DEFICIENCY OF 7S GAMMA-GLOBULINS IN THE PRESENCE OF ELEVATED 19S GAMMA-GLOBULINS

1961 • 185 citations

Five polymorphic microsatellite VNTRs on the human X chromosome.

1990 • 164 citations

Evidence for a Defect in Switch T Cells in Patients with Immunodeficiency and Hyperimmunoglobulinemia M

1986 • 126 citations

Close linkage of random DNA fragments from Xq 21.3–22 to X-linked agammaglobulinaemia (XLA)

1987 • 57 citations

Mapping of the x-linked form of hyper-IgM syndrome (HIGM1) to Xq26 by close linkage to HPRT

1992 • 57 citations

Yeast artificial chromosomes spanning 8 megabases and 10-15 centimorgans of human cytogenetic band Xq26.

1992 • 53 citations

X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus

1987 • 53 citations

Genetic mapping of four dinucleotide repeat loci, DXS453, DXS458, DXS454, and DXS424, on the X chromosome using multiplex polymerase chain reaction

1992 • 52 citations

Evidence that in X‐linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intact

1990 • 50 citations

Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26).

1991 • 37 citations

Genetic and physical mapping of Xq24–q26 markers flanking the Lowe oculocerebrorenal syndrome

1990 • 36 citations

Tetranucleotide repeat polymorphism at the HPRT locus

1991 • 35 citations

A Family with Several Cases of Hypogammaglobulinaemia

1962 • 21 citations

Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages

1991 • 18 citations

Genetics of human X-linked immunodeficiency diseases

1991 • 11 citations

[Arterial steal via an arteriovenous fistula for hemodialysis. A clinical case and review of the literature].

1993 • 1 citations