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    Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report) by Zul Qarnain, Fatima Khan, Fizza Akbar, Salman Kirmani

    Published 2022-01-01
    “…We report a novel loss-of-function homozygous variant in TTI2 that leads to syndromic intellectual disability and primary microcephaly.…”
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    Where are Our Educators? by Елізабет Тюнс, Зоя Рібейро Престес

    Published 2024-12-01
    Subjects: “…social networks, social relationships, intellectual and personality development.…”
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