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Predictor(s) of Abnormal Array Comparative Genomic Hybridization Results in Patients With Cleft Lip and/or Palate.Molecular analysis of the novel IDS allele in a Thai family with mucopolysaccharidosis type II: The c.928C>T (p.Gln310*) transcript is sensitive to nonsense-mediated mRNA decay.Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder.Classic phenotype of Coffin-Lowry syndrome in a female with stimulus-induced drop episodes and a genotype with preserved N-terminal kinase domain.Congenital central hypoventilation syndrome mimicking mitochondrial disease.Craniosynostosis and radial ray defect: a rare presentation of 22q11.2 deletion syndromeStudying Down syndrome recognition probabilities in Thai children with de-identified computer-aided facial analysisOxygen saturation trends in preterm infants during the first 15 min after birthSex-discordant monochorionic twins with blood and tissue chimerismHajdu-Cheney syndrome: phenotypical progression with de-novo NOTCH2 mutationQuality of life and comprehensive health supervision for children with Down syndrome in ThailandClinical course, mutations and its functional characteristics of infantile-onset Pompe disease in ThailandIdentification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome SequencingClinical delineation of 18q11-q12 microdeletion: Intellectual disability, speech and behavioral disorders, and conotruncal heart defects
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Q41712154-54D57B32-6E34-4362-8A02-20177AA244E6Q42235416-B2570486-7C99-42BC-AB0C-43FE81665CDCQ42362268-CE1ED979-9873-4914-A2AF-E755A14BD0DCQ54392171-A4B9219F-72F2-4804-8F7F-8E9D699705F7Q54970278-0C5470BE-19F5-4F00-B932-704E7815BA5AQ56266967-B00E008F-FBC6-4673-9910-46348366D2A4Q62495046-422642DF-14EE-4601-B221-C73BE3CC387EQ84849545-8D5C01FB-B44C-4705-A202-81F1CDE4F571Q86814795-3396EB5D-CBE2-404D-9C26-336EECE98DDBQ87415254-B66AEDA1-1AF7-4839-A147-5A760E71CA7CQ89846285-C75E9C75-F8A0-4180-B524-1EDB8CCB2C2CQ90066296-01928E14-4D32-46DA-973F-99F8E5F0FF82Q91236678-0A9F7953-396B-4139-AF8D-9F4355795310Q92474686-FDAEA764-83B0-4C22-8900-94FF752169FE
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description
investigador
@es
researcher
@en
name
K Rojnueangnit
@en
type
label
K Rojnueangnit
@en
prefLabel
K Rojnueangnit
@en
P31
P496
0000-0002-9488-4470