A rare homozygous ALX4 mutation in a Bangladeshi girl with frontonasal dysplasia type-2 (FND2).
Goswami B, Rahman A, Jahan I, Akter S, Banu TA, Osman E, Uzzaman MS, Habib A, Alam MS, Mohammad Abu Obaida AS, Hasan Sarkar MM, Khan S.
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Heliyon. 2024 Jul 20;10(15):e34929. doi: 10.1016/j.heliyon.2024.e34929. eCollection 2024 Aug 15.
Heliyon. 2024.
PMID: 39157323
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