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By Tohyama Jun  

Human Molecular Genetics, Vol. 9, Iss. 11, 2000-07 ,pp. : 1699-1707

Oxford University Press

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Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex

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Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 3037-3046

Oxford University Press

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A statistical model for dissecting genomic imprinting through genetic mapping

By Cui Yuehua   Cheverud James   Wu Rongling  

Genetica, Vol. 130, Iss. 3, 2007-07 ,pp. : 227-239

Springer Publishing Company

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Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of Tuberous Sclerosis Complex

By Zeng Ling-Hui   Rensing Nicholas R.   Zhang Bo   Gutmann David H.   Gambello Michael J.   Wong Michael  

Human Molecular Genetics, Vol. 20, Iss. 3, 2011-02 ,pp. : 445-454

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Computer-Assisted Phenotype Characterization for Genetic Research in Psychiatry

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Human Heredity, Vol. 58, Iss. 3-4, 2005-03 ,pp. : 122-130

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