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Tim Phetthong

1PUBLICATIONS

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Optical technology

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|Oct 23, 2021

Compound Heterozygote of Point Mutation and Chromosomal Microdeletion Involving <i>OTUD6B</i> Coinciding with <i>ZMIZ1</i> Variant in Syndromic Intellectual Disability.

Tim Phetthong, Arthaporn Khongkrapan, Natini Jinawath

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Duangrurdee Wattanasirichaigoon

Frequent Collaborators

1 joint publications

Duangrurdee Wattanasirichaigoon

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