Hongke Ding
Guangzhou, 511400, China
Last Updated: 09/26/2026
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Found 34 publications
Prenatal Genetic and Sonographic Features of KBG Syndrome: A Cohort Study of 19 Fetal Cases.
Journal: Prenatal diagnosis
Published: February 02, 2026
Identification of a novel de novo NONO variants causing X-linked syndromic intellectual developmental disorder-34 in a fetus.
Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: November 01, 2025
Clinical utility of exome sequencing in hearing loss: a retrospective cohort study.
Journal: Frontiers in genetics
Published: June 09, 2025
A case of primary microcephaly associated with compound heterozygous variants of WDR62 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 11, 2025
OSGEP-associated Galloway-Mowat syndrome: a longitudinal genotype-phenotype correlation from prenatal imaging markers to lifespan neurologic-renal trajectories.
Journal: QJM : monthly journal of the Association of Physicians
Published: May 06, 2025
Utility of whole exome sequencing in the evaluation of isolated fetal growth restriction in normal chromosomal microarray analysis.
Journal: Annals of medicine
Published: March 11, 2025
ALG8-CDG: advances in molecular and prenatal phenotyping facilitate prenatal diagnosis and genetic counseling.
Journal: QJM : monthly journal of the Association of Physicians
Published: November 20, 2024
Exome sequencing for nonimmune hydrops fetalis and clinical utility of data reanalysis.
Journal: QJM : monthly journal of the Association of Physicians
Published: August 06, 2024
High positive predictive value of CNVs detected by clinical exome sequencing in suspected genetic diseases.
Journal: Journal of translational medicine
Published: April 07, 2024
Last Updated: 09/26/2026