Duangrurdee Wattanasirichaigoon

Rama 6 Road
Bangkok, 10400, Thailand

Last Updated: 09/26/2026

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Found 76 publications

Prenatal Whole-Genome Sequencing for Fetal Anomalies: Diagnostic Performance, Challenges, and Clinical Implications.

Prenatal Whole-Genome Sequencing for Fetal Anomalies: Diagnostic Performance, Challenges, and Clinical Implications.

Journal: International journal of molecular sciences

Published: March 03, 2026

A case with a de novo chromosome 8.9 Mb 11pter duplication and 6.4 Mb 11qter deletion derived from a father with a normal karyotype.

A case with a de novo chromosome 8.9 Mb 11pter duplication and 6.4 Mb 11qter deletion derived from a father with a normal karyotype.

Journal: Clinical dysmorphology

Published: November 06, 2025

High depth targeted next-generation sequencing in vascular malformations.

High depth targeted next-generation sequencing in vascular malformations.

Journal: Human molecular genetics

Published: August 06, 2025

Application of Prenatal Whole Exome Sequencing for Congenital Heart Anomalies.

Application of Prenatal Whole Exome Sequencing for Congenital Heart Anomalies.

Journal: International journal of molecular sciences

Published: July 17, 2025

Clinical performance of expanded non-invasive prenatal testing for aneuploidies: a real-world experience in Thailand.

Clinical performance of expanded non-invasive prenatal testing for aneuploidies: a real-world experience in Thailand.

Journal: BMC pregnancy and childbirth

Published: July 13, 2025

Impacts and Economic Burden of Pompe Disease on Patients and Families in Thailand: A Mixed Method Study.

Impacts and Economic Burden of Pompe Disease on Patients and Families in Thailand: A Mixed Method Study.

Journal: ClinicoEconomics and outcomes research : CEOR

Published: May 22, 2025

Expanding the clinical and molecular spectrum of TBC1D32-related ciliopathy: case reports and literature Review.

Expanding the clinical and molecular spectrum of TBC1D32-related ciliopathy: case reports and literature Review.

Journal: Journal of human genetics

Published: April 09, 2025

Assessing the Value for Money of Enzyme Replacement Therapy in Gaucher Disease Types 1 and 3b: Can Expanded Coverage Be Justified?

Assessing the Value for Money of Enzyme Replacement Therapy in Gaucher Disease Types 1 and 3b: Can Expanded Coverage Be Justified?

Journal: PharmacoEconomics - open

Published: April 08, 2025

HMG-CoA Synthase-2 Deficiency: Neonatal Hyperammonemic Coma and Abnormal Metabolic Screening Resembling Maple Syrup Urine Disease.

HMG-CoA Synthase-2 Deficiency: Neonatal Hyperammonemic Coma and Abnormal Metabolic Screening Resembling Maple Syrup Urine Disease.

Journal: JIMD reports

Published: April 05, 2025

Diagnostic yield of whole exome sequencing with targeted gene analysis in prelingual sensorineural hearing loss in Thailand.

Diagnostic yield of whole exome sequencing with targeted gene analysis in prelingual sensorineural hearing loss in Thailand.

Journal: Scientific reports

Published: March 17, 2025

Early neonatal death due to prenatally undiagnosed congenital subglottic stenosis in Noonan syndrome.

Early neonatal death due to prenatally undiagnosed congenital subglottic stenosis in Noonan syndrome.

Journal: BMC pregnancy and childbirth

Published: February 14, 2025

Prenatal carrier screening for spinal muscular atrophy among pregnant Thai women.

Prenatal carrier screening for spinal muscular atrophy among pregnant Thai women.

Journal: Frontiers in medicine

Published: January 24, 2025

Showing 1-12 of 76

Last Updated: 09/26/2026