Jinjie Pan
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
Case Report: Prenatal diagnosis of a rare complex fetal karyotype 47,U,t(10;13)(p15;q22)mat,+der(13)t(10;13)dmat resulting from 3:1 meiotic segregation of a maternal balanced translocation.
Journal: Frontiers in reproductive health
Published: November 01, 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 First Compound Heterozygosity for Two Different α-Thalassemia Determinants Causes Hb Bart's Hydrops Fetalis in a Chinese Family.
Journal: Hemoglobin
Published: December 18, 2024
Interaction of smoking and aging on emphysema and small airways disease in asymptomatic healthy men by CT-based parametric response mapping analysis.
Journal: Clinical radiology
Published: May 19, 2023
A novel rearrangement of the α-globin gene cluster containing both the -α3.7 and ααααanti4.2 crossover junctions in a Chinese family.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: February 16, 2022
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Last Updated: 09/26/2026