Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII.

od Jackson, C L, Bruns, G A, Breslow, J L
Izdano 1984

A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37.

od Litt, M, Bruns, G A, Sheehy, R, Magenis, R E
Izdano 1986

Mapping of the human APOB gene to chromosome 2p and demonstration of a two-allele restriction fragment length polymorphism.

od Huang, L S, Miller, D A, Bruns, G A, Breslow, J L
Izdano 1986

An anonymous DNA segment (II227) maps to the long arm of human chromosome 5 and identifies a BstXI polymorphism (D5S26).

od Stewart, G D, Bruns, G A, Wasmuth, J J, Kurnit, D M
Izdano 1987

Localization of gelsolin proximal to ABL on chromosome 9.

od Kwiatkowski, D J, Westbrook, C A, Bruns, G A, Morton, C C
Izdano 1988

The major human erythroid DNA-binding protein (GF-1): primary sequence and localization of the gene to the X chromosome.

od Zon, L I, Tsai, S F, Burgess, S, Matsudaira, P, Bruns, G A, Orkin, S H
Izdano 1990

Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.

od Dinauer, M C, Pierce, E A, Bruns, G A, Curnutte, J T, Orkin, S H
Izdano 1990

Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19.

od Bufton, L, Bruns, G A, Magenis, R E, Tomar, D, Shaw, D, Brook, D, Litt, M
Izdano 1986

Human inhibitor of the first component of complement, C1: characterization of cDNA clones and localization of the gene to chromosome 11.

od Davis, A E, Whitehead, A S, Harrison, R A, Dauphinais, A, Bruns, G A, Cicardi, M, Rosen, F S
Izdano 1986

Molecular characterization of sialophorin (CD43), the lymphocyte surface sialoglycoprotein defective in Wiskott-Aldrich syndrome.

od Shelley, C S, Remold-O'Donnell, E, Davis, A E, Bruns, G A, Rosen, F S, Carroll, M C, Whitehead, A S
Izdano 1989

A deletion map of the WAGR region on chromosome 11.

od Gessler, M, Thomas, G H, Couillin, P, Junien, C, McGillivray, B C, Hayden, M, Jaschek, G, Bruns, G A
Izdano 1989

The gene encoding the epsilon subunit of the T3/T-cell receptor complex maps to chromosome 11 in humans and to chromosome 9 in mice.

od Gold, D P, van Dongen, J J, Morton, C C, Bruns, G A, van den Elsen, P, Geurts van Kessel, A H, Terhorst, C
Izdano 1987

Role for the Wilms tumor gene in genital development?

od van Heyningen, V, Bickmore, W A, Seawright, A, Fletcher, J M, Maule, J, Fekete, G, Gessler, M, Bruns, G A, Huerre-Jeanpierre, C, Junien, C
Izdano 1990

Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)

od Bach, I., Brunner, H. G., Beighton, P., Ruvalcaba, R. H. A., Reardon, W., Pembrey, M. E., van der Velde-Visser, S. D., Bruns, G. A. P., Cremers, C. W. R. J., Cremers, F. P. M., Ropers, H.-H.
Izdano 1992