A Kinesin Heavy Chain ( KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10) von 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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Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects von 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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Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432 von SPEER, Marcy C, GRAHAM, Felicia Lennon, BONNER, Erin, COLLIER, Keva, STAJICH, Jeffrey M, GASKELL, Perry C, PERICAK-VANCE, Margaret A, VANCE, Jeffery M

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Identification of a New Autosomal Dominant Limb-Girdle Muscular Dystrophy Locus on Chromosome 7 von 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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Current Prevalence of Specific Clinical Outcomes in Adult Patients with Hb SS or Hb Sβ0 Thalassemia von De Castro, Laura M., Lennon-Graham, Felicia C., Ashley-Koch, Allison G., Jonassaint, Jude C., Eckman, James J., Orringer, Eugene P., Telen, Marilyn J.

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

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Priapism in SCD: Clinical and Genetic Correlations von 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.

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Genetic Polymorphisms Associated with Risk for Pulmonary Hypertension and Proteinuria in Sickle Cell Disease von 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.

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Exclusion of Identified LGMD1 Loci from Four Dominant Limb-Girdle Muscular Dystrophy Families von 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.

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