Pages that link to "Q73981596"
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The following pages link to Re: prostate cancer susceptibility locus on chromosome 1q: a confirmatory study (Q73981596):
Displaying 33 items.
- Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer (Q24536433) (← links)
- Molecular biology of prostate carcinogenesis (Q33816588) (← links)
- A genome screen of families with multiple cases of prostate cancer: evidence of genetic heterogeneity (Q34020369) (← links)
- Model-free linkage analysis with covariates confirms linkage of prostate cancer to chromosomes 1 and 4. (Q34020687) (← links)
- Segregation analyses of 1,476 population-based Australian families affected by prostate cancer (Q34020691) (← links)
- Genetics of prostate cancer: too many loci, too few genes (Q34078064) (← links)
- A genomic scan of families with prostate cancer identifies multiple regions of interest (Q34141779) (← links)
- Evidence for a prostate cancer-susceptibility locus on chromosome 20. (Q34141928) (← links)
- Linkage analyses at the chromosome 1 loci 1q24-25 (HPC1), 1q42.2-43 (PCAP), and 1p36 (CAPB) in families with hereditary prostate cancer (Q34145106) (← links)
- A genome screen of multiplex sibships with prostate cancer. (Q34145438) (← links)
- Combined analysis of hereditary prostate cancer linkage to 1q24-25: results from 772 hereditary prostate cancer families from the International Consortium for Prostate Cancer Genetics (Q34145444) (← links)
- Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36. (Q34389120) (← links)
- Analysis of chromosome 1q42.2-43 in 152 families with high risk of prostate cancer (Q34389363) (← links)
- In Swedish families with hereditary prostate cancer, linkage to the HPC1 locus on chromosome 1q24-25 is restricted to families with early-onset prostate cancer (Q34390802) (← links)
- Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion (Q34390891) (← links)
- Prostate cancer genomics (Q34707619) (← links)
- New insights and candidate genes and their implications for care of patients with hereditary prostate cancer (Q34707800) (← links)
- Genetic susceptibility to prostate cancer: a review. (Q35566211) (← links)
- Inherited predisposition to prostate cancer (Q35585517) (← links)
- Identification of a prostate cancer susceptibility locus on chromosome 7q11-21 in Jewish families (Q36604157) (← links)
- No evidence of linkage to chromosome 1q42.2-43 in 131 prostate cancer families from the ACTANE consortium. Anglo, Canada, Texas, Australia, Norway, EU Biomed (Q36621593) (← links)
- The clinical genetics of prostate cancer (Q39485394) (← links)
- Genome‐wide scan of Swedish families with hereditary prostate cancer: Suggestive evidence of linkage at 5q11.2 and 19p13.3 (Q42612590) (← links)
- PCAP is the major known prostate cancer predisposing locus in families from south and west Europe (Q48906885) (← links)
- Heterogeneity in genetic susceptibility to prostate cancer (Q49034145) (← links)
- Men's attitudes regarding genetic testing for hereditary prostate cancer risk. (Q52171337) (← links)
- Evidence for a prostate cancer susceptibility locus on the X chromosome. (Q57274826) (← links)
- Autosomal dominant inheritance of prostate cancer: a confirmatory study (Q57307295) (← links)
- Replication linkage study for prostate cancer susceptibility genes (Q73066893) (← links)
- Familial and hereditary prostate cancer in southern Sweden. A population-based case-control study (Q78128611) (← links)
- Genetic epidemiology of prostate cancer (Q78169776) (← links)
- Genetic fieldwork for hereditary prostate cancer studies (Q78635746) (← links)
- Where are the prostate cancer genes?—A summary of eight genome wide searches (Q79255939) (← links)