Search Results - Kulalı, Melike Ataseven

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  1. 1
    A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis

    A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis by Kırkgöz, Tarık, Özkan, Behzat, Hazan, Filiz, Acar, Sezer, Nalbantoğlu, Özlem, Özkaya, Beyhan, Kulalı, Melike Ataseven, Gürsoy, Semra, Ikegawa, Shiro, Guo, Long

    Published in Frontiers in genetics
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  2. 2
    Type A insulin resistance syndrome due to a novel heterozygous c.3486_3503del (p. Arg1163_Ala1168del) INSR gene mutation in an adolescent girl and her mother

    Type A insulin resistance syndrome due to a novel heterozygous c.3486_3503del (p. Arg1163_Ala1168del) INSR gene mutation in an adolescent girl and her mother by Koca, Serkan Bilge, Kulali, Melike Ataseven, Güğüş, Başak, Demirbilek, Hüseyin

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  3. 3
    ITPA related developmental encephalopathy: Key role of neuroimaging

    ITPA related developmental encephalopathy: Key role of neuroimaging by Çavusoglu, Dilek, Kulali, Melike, Dündar, Nihal, Gokaslan, Cigdem, Aydin, Kurşad

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