Search Results - Tolun, Aslhan

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  1. 1
    DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability

    DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability by Köroğlu, Çiğdem, Baysal, Leyla, Cetinkaya, Murat, Karasoy, Hatice, Tolun, Aslhan

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  2. 2
    A homozygous 237-kb deletion at 1p31 identified as the locus for midline cleft of the upper and lower lip in a consanguineous family

    A homozygous 237-kb deletion at 1p31 identified as the locus for midline cleft of the upper and lower lip in a consanguineous family by Yıldırım, Yeşerin, Kerem, Metin, Köroğlu, Çiğdem, Tolun, Aslıhan

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  3. 3
    A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood

    A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood by Lohmann, Ebba, Köroğlu, Çiğdem, Hanagasi, Hasmet A, Dursun, Burcu, Taşan, Erşan, Tolun, Aslhan

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  4. 4
    Early-Onset Progressive Myoclonic Epilepsy With Dystonia Mapping to 16pter-p13.3

    Early-Onset Progressive Myoclonic Epilepsy With Dystonia Mapping to 16pter-p13.3 by Duru, Nadire, Iseri, Sibel Aylin Ugur, Selç, Nilgün, Tolun, Asl han

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