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1 iated with a significantly increased risk of hereditary prostate cancer.
2 A total of 74 North American families with hereditary prostate cancer.
6 The RNASEL gene, a strong candidate for the hereditary prostate cancer 1 allele (HPC1), encodes a si
8 ified as a candidate susceptibility gene for hereditary prostate cancer and as a risk factor for spor
9 e 1q24-25 region in 772 families affected by hereditary prostate cancer and ascertained by the member
10 NKX3.1 may play a role in susceptibility to hereditary prostate cancer and underscore a role for NKX
11 r accentuated among men meeting criteria for hereditary prostate cancer, and further still for those
12 r study shows that a significant fraction of hereditary prostate cancers are diagnosed in advanced st
14 ine mapping linkage analysis at 8p among 206 hereditary prostate cancer families also provided eviden
15 sequenced the NKX3.1 gene in 159 probands of hereditary prostate cancer families recruited at Johns H
16 amilies, which represent a stratification of hereditary prostate cancer families with potentially inc
17 ases and 222 controls) and family-based (159 hereditary prostate cancer families) association study w
18 y genome-wide scans, encompassing some 1,500 hereditary prostate cancer families, indicate that prost
20 d with prostate cancer risk in families with hereditary prostate cancer (HPC) and in patients with no
21 reviously performed a genome-wide search for hereditary prostate cancer (HPC) genes, finding evidence
24 nd linkage studies in families affected with hereditary prostate cancer (HPC) have implicated this re
26 nd prostate cancer susceptibility in several hereditary prostate cancer (HPC) populations, we hypothe
27 nkage analyses, in 159 pedigrees affected by hereditary prostate cancer (HPC), using 24 markers on th
29 C2/ELAC2 gene at 17p11 in 159 pedigrees with hereditary prostate cancer (HPC); (2) a mutation-screeni
31 A 10-cM genomewide scan of 94 families with hereditary prostate cancer, including 432 affected men,
33 small proportion of all families affected by hereditary prostate cancer, it appears to play a more pr
34 ided by the identification of other putative hereditary prostate cancer loci on Xq27-28, 1q42-43, and
36 dentify the susceptibility genes involved in hereditary prostate cancer (OMIM 176807) and hyperparath
39 NPs were further genotyped in a total of 159 hereditary prostate cancer probands, 245 sporadic prosta
42 mine if these loci were also associated with hereditary prostate cancer, we genotyped them in a famil