Chia-cheng Hung
TPQ, Taiwan
Last Updated: 09/26/2026
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Found 10 publications
Screening for Hearing Impairment in Newborns Using Targeted Genomic Sequencing: A Large Pilot Cohort Study.
Journal: Clinical and experimental otorhinolaryngology
Published: September 13, 2024
MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia.
MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia.
Journal: Scientific reports
Published: December 26, 2019
TP53 alterations in relapsed childhood acute lymphoblastic leukemia.
Journal: Cancer science
Published: September 18, 2019
Fragile X syndrome carrier screening in pregnant women in Chinese Han population.
Journal: Scientific reports
Published: January 29, 2019
Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan.
Journal: The Journal of pediatrics
Published: December 21, 2017
Newborn genetic screening for hearing impairment: a population-based longitudinal study.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 06, 2016
Targeted next-generation sequencing of cancer genes identified frequent TP53 and ATRX mutations in leiomyosarcoma.
Journal: American journal of translational research
Published: August 08, 2015
Probable high prevalence of limb-girdle muscular dystrophy type 2D in Taiwan.
Journal: Journal of the neurological sciences
Published: July 13, 2015
Blastocyst biopsy and vitrification are effective for preimplantation genetic diagnosis of monogenic diseases.
Journal: Human reproduction (Oxford, England)
Published: March 14, 2013
A feasible strategy of preimplantation genetic diagnosis for carriers with chromosomal translocation: Using blastocyst biopsy and array comparative genomic hybridization.
Journal: Journal of the Formosan Medical Association = Taiwan yi zhi
Published: September 28, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026