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Zul Qarnain

1PUBLICATIONS

1CO-AUTHORS

Genetics not elsewhere classified

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Publications (1)

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|Aug 22, 2022

Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report).

Zul Qarnain, Fatima Khan, Fizza Akbar

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Salman Kirmani

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Salman Kirmani

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