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Chromosomal abnormalities study for anembryonic pregnancy by BACs-on-Beads technique.
Eur J Obstet Gynecol Reprod Biol. 2024 Apr 30;298:31-34. doi: 10.1016/j.ejogrb.2024.04.041. Online ahead of print.
Eur J Obstet Gynecol Reprod Biol. 2024.
PMID: 38705011
The Utilization of MS-MLPA as the First-Line Test for the Diagnosis of Prader-Willi Syndrome in Thai Patients.
Prapasrat C, Onsod P, Korkiatsakul V, Rerkamnuaychoke B, Wattanasirichaigoon D, Chareonsirisuthigul T.
Prapasrat C, et al. Among authors: onsod p.
J Pediatr Genet. 2022 Jan 7;12(4):273-279. doi: 10.1055/s-0041-1741008. eCollection 2023 Dec.
J Pediatr Genet. 2022.
PMID: 38162164
Free PMC article.
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Clinical Features to Predict 22q11.2 Deletion Syndrome Proven by Molecular Genetic Testing.
Rojnueangit K, Khetkham T, Onsod P, Chareonsirisuthigul T.
Rojnueangit K, et al. Among authors: onsod p.
J Pediatr Genet. 2020 Oct 1;11(1):22-27. doi: 10.1055/s-0040-1718386. eCollection 2022 Mar.
J Pediatr Genet. 2020.
PMID: 35186386
Free PMC article.
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Performance of the MLPA technique for detecting common mutations in Leber hereditary optic neuropathy.
Dokrungkoon T, Onsod P, Areesirisuk P, Rerkamnuaychoke B, Vanikieti K, Chareonsirisuthigul T.
Dokrungkoon T, et al. Among authors: onsod p.
Mitochondrial DNA A DNA Mapp Seq Anal. 2019 Dec;30(8):819-824. doi: 10.1080/24701394.2019.1670819. Epub 2019 Sep 28.
Mitochondrial DNA A DNA Mapp Seq Anal. 2019.
PMID: 31566038
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The Utilization of Karyotyping, iFISH, and MLPA for the Detection of Recurrence Genetic Aberrations in Multiple Myeloma.
Sommaluan S, Rerkamnuaychoke B, Pauwilai T, Chancharunee S, Onsod P, Pornsarayuth P, Chareonsirisuthigul T, Tammachote R, Siriboonpiputtana T.
Sommaluan S, et al. Among authors: onsod p.
Asian Pac J Cancer Prev. 2017 Nov 26;18(11):3135-3142. doi: 10.22034/APJCP.2017.18.11.3135.
Asian Pac J Cancer Prev. 2017.
PMID: 29172291
Free PMC article.
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