8 results on '"Willett-Brozick, J.E."'
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2. Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. (Original Article)
3. Evidence for recurrent deletions spanning the SDHC gene at chromosome 1q21 in families with hereditary paraganglioma type 3 (PGL3)
4. Effect of altitude on the clinical severity of hereditary paraganglioma
5. DIBD1, a novel gene homologous to Saccaromyces cerevisiae ALG9, is disrupted in a family with bipolar affective disorder by a translocation breakpoint at 11q23
6. Genomic analysis of the breakpoints in balanced t(9;11)(p24;q23.1) translocation that partially co-segregates with bipolar affective disorder in a small family
7. SDHD gene testing in 'sporadic' paraganglioma indicates a high proportion of unrecognized heritable cases
8. Genetic heterogeneity in hereditary paraganglioma (PGL): SDHD is the primary locus in imprinted PGL pedigrees
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