Cognitive impairment in Coffin-Lowry syndrome correlates with reduced RSK2 activation von HARUM, Karen H, ALEMI, Lily, JOHNSTON, Michael V

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Learning, memory, and transcription factors von JOHNSTON, Michael V, ALEMI, Lily, HARUM, Karen H

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Homozygous factor-V mutation as a genetic cause of perinatal thrombosis and cerebral palsy von Harum, Karen H, Hoon, Alexander H, Kato, Gregory J, Casella, James F, Breiter, Steven N, Johnston, Michael V

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Factor-V Leiden: a risk factor for cerebral palsy von Harum, Karen H, Hoon, Alexander H, Casella, James F

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Children's Participation in Genetic Prevalence Research: Influences on Enrollment and Reports of Parent Satisfaction1 von Mazzocco, Michèle M. M., Myers, Gwen F., Harum, Karen H., Reiss, Allan L.

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Children's Participation in Genetic Prevalence Research: Influences on Enrollment and Reports of Parent Satisfaction von Mazzocco, Michèle M. M., Myers, Gwen F., Harum, Karen H., Reiss, Allan L.

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Factor‐V Leiden: a risk factor for cerebral palsy von Harum, Karen H, Hoon, Alexander H, Casella, James F

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Recent progress in the neurology of learning : Memory molecules in the developing brain von JOHNSTON, M. V, HARUM, K. H

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Kinase Activity: Phenotype Correlation in Coffin-Lowry Syndrome 716 von Harum, Karen H, Johnston, Michael V, Ginty, David D

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Homozygous factor‐V mutation as a genetic cause of perinatal thrombosis and cerebral palsy von Harum, Karen H, Hoon, Alexander H, Kato, Gregory J, Casella, James F, Breiter, Steven N, Johnston, Michael V

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Children's Participation in Genetic Prevalence Research: Influences on Enrollment and Reports of Parent Satisfaction 1 von Mazzocco, Michèle M. M., Myers, Gwen F., Harum, Karen H., Reiss, Allan L.

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Developmental neurobiology: New concepts in learning, memory, and neuronal development von Harum, Karen H., Johnston, Michael V.

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Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients von Doheny, K F, McDermid, H E, Harum, K, Thomas, G H, Raymond, G V

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Inherited duplication Xq27-qter at Xp22.3 in severely affected males: Molecular cytogenetic evaluation and clinical description in three unrelated families von Goodman, Barbara K., Shaffer, Lisa G., Rutberg, Julie, Leppert, Mary, Harum, Karen, Gagos, Sarantis, Ray, James H., Bialer, Martin G., Zhou, Xianting, Pletcher, Beth A., Shapira, Stuart K., Geraghty, Michael T.

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