Chaiyasap P - Search Results

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Whole genome and exome sequencing of monozygotic twins with trisomy 21, discordant for a congenital heart defect and epilepsy.

Chaiyasap P, Kulawonganunchai S, Srichomthong C, Tongsima S, Suphapeetiporn K, Shotelersuk V. Chaiyasap P, et al. PLoS One. 2014 Jun 20;9(6):e100191. doi: 10.1371/journal.pone.0100191. eCollection 2014. PLoS One. 2014. PMID: 24950249 Free PMC article.

Massive parallel sequencing as a new diagnostic approach for phenylketonuria and tetrahydrobiopterin-deficiency in Thailand.

Chaiyasap P, Ittiwut C, Srichomthong C, Sangsin A, Suphapeetiporn K, Shotelersuk V. Chaiyasap P, et al. BMC Med Genet. 2017 Sep 16;18(1):102. doi: 10.1186/s12881-017-0464-x. BMC Med Genet. 2017. PMID: 28915855 Free PMC article.

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