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Expansion of phenotypic and genotypic data in autism spectrum disorders due to variants in the CHD8 gene.
Neurogenetics. 2024 Nov 22;26(1):4. doi: 10.1007/s10048-024-00781-9.
Neurogenetics. 2024.
PMID: 39576488
Auditory Phenotype of a Novel Missense Variant in the CEACAM16 Gene in a Large Russian Family With Autosomal Dominant Nonsyndromic Hearing Loss.
Markova TG, Alekseeva NN, Ryzhkova OP, Shatokhina OL, Orlova AA, Zabnenkova VV, Groznova OS, Sagaydak OV, Chibisova SS, Polyakov AV, Tavartkiladze GA.
Markova TG, et al. Among authors: groznova os.
J Int Adv Otol. 2024 Mar 27;20(2):119-126. doi: 10.5152/iao.2024.231252.
J Int Adv Otol. 2024.
PMID: 39157884
Free PMC article.
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