Guosheng Deng
Yulin, China
Last Updated: 09/26/2026
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Found 9 publications
Correction: A rare case of mosaic partial tetrasomy 18p presenting with oligomenorrhea and intellectual disability: a case report.
Journal: Frontiers in medicine
Published: February 03, 2026
Case Report: Prenatal genetic analysis of a rare fetus with 45, X/46, X, dic r (Y; Y)/46, X, r(Y) karyotype.
Journal: Frontiers in genetics
Published: December 02, 2025
Fertility preservation in turner syndrome: a case report integrating clinical presentation with genomic and molecular mechanistic analyses.
Journal: Journal of assisted reproduction and genetics
Published: November 23, 2025
Optimizing the diagnostic approach for sex chromosome and autosomal mosaicism in amniotic fluid: integrating karyotyping with CNV-seq.
Journal: Journal of assisted reproduction and genetics
Published: November 22, 2025
Genetic analysis of a fetus with mosaic trisomy 15 with false-negative result in prenatal amniotic fluid karyotype analysis.
Journal: Taiwanese journal of obstetrics & gynecology
Published: April 14, 2025
Prevalence, spermatozoa, hormonal, and genetic evaluation of rare mosaic klinefelter syndrome patients in southern China.
Journal: Frontiers in genetics
Published: February 08, 2025
The effect of overnight culture after thawing of D3 cleavage-stage embryos on clinical pregnancy outcomes: focus on embryo development to day 4.
Journal: Frontiers in endocrinology
Published: November 18, 2024
Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder.
Journal: Molecular cytogenetics
Published: February 12, 2020
Showing 1-9 of 9
Last Updated: 09/26/2026