Search Results - "Lind, Tammy"

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  1. 1

    Germline mutations in Peruvian patients with hemophilia B: Pattern of mutation in AmerIndians is similar to the putative endogenous germline pattern by Heit, John A., Thorland, Erik C., Ketterling, Rhett P., Lind, Tammy J., Daniels, Todd M., Zapata, Renee Eyzaguirre, Ordonez, Saul Mendoza, Kasper, Carol K., Sommer, Steve S.

    Published in Human mutation (1998)
    “…Exogenous (e.g., environmental) mutagens produce characteristic patterns of mutation. In contrast, endogenous mutation processes likely are associated with an…”
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  2. 2

    The human factor IX gene as germline mutagen test: Samples from mainland China have the putatively endogenous pattern of mutation by Liu, Jing-Zhong, Li, Xuemin, Drost, Joni, Thorland, Erik C., Liu, Qiang, Lind, Tammy, Roberts, Stacy, Wang, H.Y., Sommer, Steve S.

    Published in Human mutation (01-07-2000)
    “…Germline mutations are the major source of genetic variation that allows a species to evolve over time but at the cost of Mendelian disease and genetic…”
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  3. 3

    The D5 dopamine receptor gene in schizophrenia: identification of a nonsense change and multiple missense changes but lack of association with disease by Sobell, J L, Lind, T J, Sigurdson, D C, Zald, D H, Snitz, B E, Grove, W M, Heston, L L, Sommer, S S

    Published in Human molecular genetics (01-04-1995)
    “…To determine whether mutations in the D5 dopamine receptor gene (DRD5) are associated with schizophrenia, the gene was examined in 78 unrelated schizophrenic…”
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  4. 4

    Screening the monoamine oxidase B gene in 100 male patients with schizophrenia: A cluster of polymorphisms in African-Americans but lack of functionally significant sequence changes by Sobell, Janet L., Lind, Tammy J., Hebrink, David D., Heston, Leonard L., Sommer, Steve S.

    Published in American journal of medical genetics (21-02-1997)
    “…The monoamine oxidase B (MAO‐B) gene was examined in 100 alleles derived from 80 Caucasian, 10 African‐American, 5 Asian, and 5 Native American male patients…”
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  5. 5

    The rates and patterns of deletions in the human factor IX gene by KETTERLING, R. P, VIELHABER, E. L, LIND, T. J, THORLAND, E. C, SOMMER, S. S

    Published in American journal of human genetics (01-02-1994)
    “…Deletions are commonly observed in genes with either segments of highly homologous sequences or excessive gene length. However, in the factor IX gene and in…”
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  6. 6

    Dopamine D4 receptor variants in unrelated schizophrenic cases and controls by Sommer, S S, Lind, T J, Heston, L L, Sobell, J L

    Published in American journal of medical genetics (15-07-1993)
    “…The D4 dopamine receptor (D4DR) exists in multiple allelic forms (Van Tol et al.: Nature 358:149-152, 1992) which involve different numbers of a 48 basepair…”
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