Ke Wu
Quzhou, China
Last Updated: 09/26/2026
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Found 9 publications
Prenatal diagnosis of a de novo pathogenic HNRNPK variant in a Chinese fetus with abnormal ultrasound soft markers: a case report.
Journal: Frontiers in genetics
Published: July 08, 2025
A novel frameshift STAG1 variant exhibiting haploinsufficiency due to the nonsense-mediated mRNA decay: a case report and literature review.
Journal: Frontiers in pediatrics
Published: June 19, 2025
Case Report: Prenatal diagnosis of 10 fetuses with 15q11-q13 duplication and pregnancy outcome in a cohort of Chinese women.
Journal: Frontiers in neuroscience
Published: May 06, 2025
Case Report: Identification of a novel hemizygous missense RPL10 gene variant in two unrelated patients.
Journal: Frontiers in pediatrics
Published: February 04, 2025
Lessons from a phenotypically normal infant with uniparental isodisomy of chromosome 21: a Case Report and review.
Journal: Frontiers in genetics
Published: December 13, 2024
Functional analysis of a novel homozygous missense IVD gene variant: a case report with dual genetic diagnoses.
Journal: Frontiers in pediatrics
Published: September 11, 2024
Prenatal diagnosis of dicentric chromosome X mosaicism: a case report and review.
Journal: Frontiers in genetics
Published: May 22, 2024
Prenatal diagnosis of Silver-Russell syndrome with 8q12 deletion including the PLAG1 gene: a case report and review.
Journal: Frontiers in genetics
Published: February 18, 2024
Lessons from two patients with Prader-Willi syndrome attributed to heterodisomy and isodisomy.
Journal: Pediatrics and neonatology
Published: January 30, 2024
Showing 1-9 of 9
Last Updated: 09/26/2026