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American Journal of Human Genetics|January 1, 1993
A duplicated region is responsible for the poly(ADP-ribose) polymerase polymorphism, on chromosome 13, associated with a predisposition to cancerD Lyn, B W Cherney, M Lalande, et al.
American Journal of Human Genetics|May 1, 1984
A strategy to reveal high-frequency RFLPs along the human X chromosomeJ Aldridge, L Kunkel, G Bruns, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Isolation of new probes in the region of the Wilson disease locus, 13q14.2-->q14.3P C Bull, J A Barwell, H T Hannah, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2000
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organizationJ Cavaillé, K Buiting, M Kiefmann, et al.
Genomics|March 20, 1995
Analysis of randomly amplified flow-sorted chromosomes using the polymerase chain reactionS M Hui, B Trask, G van den Engh, et al.
American Journal of Human Genetics|March 1, 1997
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3V Greger, J H Knoll, J Wagstaff, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 24, 1997
RAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 proteinR Mizuta, J M LaSalle, H L Cheng, et al.
Gene|September 16, 1996
Identification of a putative DNA replication origin in the gamma-aminobutyric acid receptor subunit beta3 and alpha5 gene cluster on human chromosome 15q11-q13, a region associated with parental imprinting and allele-specific replication timingD Sinnett, E Woolf, W Xie, et al.
Human Molecular Genetics|February 1, 1993
FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regionsJ H Knoll, D Sinnett, J Wagstaff, et al.
Human Molecular Genetics|January 15, 1999
An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNAS G Katz, S S Schneider, A Bartuski, et al.
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