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Article

Prenatal diagnosis of a 2.14-Mb familial 6q14.1 deletion encompassing the gene of HTR1B with apparently normal phenotype.

Taiwanese journal of obstetrics & gynecology - 1 Jul 2023

Chen Chih-Ping

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Share to Chromosome Deletion
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Share to Receptor, Serotonin, 5-HT1B

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PMID: 37407206
DOI: 10.1016/j.tjog.2023.05.009

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