Search Results - Graham, Felicia Lennon

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  1. 1
    A Kinesin Heavy Chain ( KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)

    A Kinesin Heavy Chain ( KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10) by Reid, Evan, Kloos, Mark, Ashley-Koch, Allison, Hughes, Lori, Bevan, Simon, Svenson, Ingrid K., Graham, Felicia Lennon, Gaskell, Perry C., Dearlove, Andrew, Pericak-Vance, Margaret A., Rubinsztein, David C., Marchuk, Douglas A.

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  2. 2
    Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects

    Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects by Vieira, Alexandre R., Murray, Jeffrey C., Trembath, Dimitri, Orioli, Iêda M., Castilla, Eduardo E., Cooper, Margaret E., Marazita, Mary L., Lennon-Graham, Felicia, Speer, Marcy

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  3. 3
    Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432

    Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432 by SPEER, Marcy C, GRAHAM, Felicia Lennon, BONNER, Erin, COLLIER, Keva, STAJICH, Jeffrey M, GASKELL, Perry C, PERICAK-VANCE, Margaret A, VANCE, Jeffery M

    Published in Neurogenetics
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  4. 4
    Current Prevalence of Specific Clinical Outcomes in Adult Patients with Hb SS or Hb Sβ0 Thalassemia

    Current Prevalence of Specific Clinical Outcomes in Adult Patients with Hb SS or Hb Sβ0 Thalassemia by De Castro, Laura M., Lennon-Graham, Felicia C., Ashley-Koch, Allison G., Jonassaint, Jude C., Eckman, James J., Orringer, Eugene P., Telen, Marilyn J.

    Published in Blood
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  5. 5
    Identification of a New Autosomal Dominant Limb-Girdle Muscular Dystrophy Locus on Chromosome 7

    Identification of a New Autosomal Dominant Limb-Girdle Muscular Dystrophy Locus on Chromosome 7 by Speer, Marcy C., Vance, Jeffery M., Grubber, Janet M., Lennon Graham, Felicia, Stajich, Jeffrey M., Viles, Kristi D., Rogala, Allison, McMichael, Robert, Chutkow, Jerry, Goldsmith, Claire, Tim, Richard W., Pericak-Vance, Margaret A.

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  6. 6
    Clinical and Genetic Profiles of the Aging Sickle Cell Patient

    Clinical and Genetic Profiles of the Aging Sickle Cell Patient by Ashley-Koch, Allison E., De Castro, Laura M., Lennon-Graham, Felicia, Jonassaint, Jude, Jackson, Terry L., Price, Jennifer, Galloway, Jason, Jones, Susan, Randall, Eldrida, Packman, Charles, Knupp, Charles, Eckman, James R., Orringer, Eugene P., Vance, Jeffery M., Telen, Marilyn J.

    Published in Blood
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  7. 7
    Priapism in SCD: Clinical and Genetic Correlations

    Priapism in SCD: Clinical and Genetic Correlations by Ashley-Koch, Allison E., De Castro, Laura M., Lennon-Graham, Felicia, Jonassaint, Jude, Jackson, Terry L., Price, Jennifer, Galloway, Jason, Jones, Susan, Randall, Eldrida, Packman, Charles, Knupp, Charles, Eckman, James R., Redding-Lallinger, Rupa, Orringer, Eugene P., Vance, Jeffery M., Telen, Marilyn J.

    Published in Blood
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  8. 8
    Genetic Polymorphisms Associated with Risk for Pulmonary Hypertension and Proteinuria in Sickle Cell Disease

    Genetic Polymorphisms Associated with Risk for Pulmonary Hypertension and Proteinuria in Sickle Cell Disease by Ashley-Koch, Allison E., De Castro, Laura, Lennon-Graham, Felicia, Jonassaint, Jude, Jackson, Terry L., Price, Jennifer, Galloway, Jason, Ataga, Ken I., Orringer, Eugene P., Vance, Jeffery M., Telen, Marilyn J.

    Published in Blood
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  9. 9
    Exclusion of Identified LGMD1 Loci from Four Dominant Limb-Girdle Muscular Dystrophy Families

    Exclusion of Identified LGMD1 Loci from Four Dominant Limb-Girdle Muscular Dystrophy Families by Speer, Marcy C., Vance, Jeffery M., Lennon-Graham, Felicia, Stajich, Jeffrey M., Viles, Kristi D., Gilchrist, James M., Nigro, Vincenzo, McMichael, Robert, Chutkow, Jerry G., Bartoloni, Lucia, Horrigan, Steven K., Westbrook, Carol A., Pericak-Vance, Margaret A.

    Published in Human heredity
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