Search Results - Heshka, Tim

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  1. 1
    Infantile metachromatic leukodystrophy (MLD) in a compound heterozygote for the c.459 + 1G > A mutation and a complete deletion of the ARSA gene

    Infantile metachromatic leukodystrophy (MLD) in a compound heterozygote for the c.459 + 1G > A mutation and a complete deletion of the ARSA gene by Eng, Barry, Heshka, Tim, Tarnopolsky, Mark A., Nakamura, Lisa M., Nowaczyk, Małgorzata J.M., Waye, John S.

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  2. 2
    Difficult prenatal diagnosis in mild Smith-Lemli-Opitz syndrome

    Difficult prenatal diagnosis in mild Smith-Lemli-Opitz syndrome by Nowaczyk, Małgorzata J.M., Heshka, Tim, Kratz, Lisa E., Kelley, Richard E.

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  3. 3
    Infantile metachromatic leukodystrophy (MLD) in a compound heterozygote for the c.459 + 1G > A mutation and a complete deletion of the ARSA gene

    Infantile metachromatic leukodystrophy (MLD) in a compound heterozygote for the c.459 + 1G > A mutation and a complete deletion of the ARSA gene by Eng, Barry, Heshka, Tim, Tarnopolsky, Mark A, Nakamura, Lisa M, Nowaczyk, Małgorzata J M, Waye, John S

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    Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p

    Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p by Xu, Jie, Freeman, Viola, Carter, Ronald F., Paes, Bosco, Heshka, Tim, Nowaczyk, Małgorzata J.M.

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