Jiebin Wu - Publications

Genetic evaluation and clinical management of subsequent pregnancies based on previous adverse obstetric history.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians

Published: December 21, 2025

Genetic Abnormalities and Clinical Management of Fetal Genitourinary System Anomalies in Eastern China.

Journal: American journal of medical genetics. Part A

Published: June 17, 2025

Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1.

Journal: Frontiers in genetics

Published: May 08, 2024

Genotype-phenotype correlations in a fetus with Kleefstra syndrome.

Journal: Taiwanese journal of obstetrics & gynecology

Published: November 13, 2023

Genetic analysis and management of a familial hypercholesterolemia pedigree with polygenic variants: Case report.

Journal: Medicine

Published: August 11, 2023

Pregnancy outcomes and genetic analysis for fetal ventriculomegaly.

Journal: Frontiers in genetics

Published: June 13, 2023

Genetic etiology and pregnancy outcomes of fetuses with central nervous system anomalies.

Journal: Archives of gynecology and obstetrics

Published: May 04, 2023

Missed diagnosis of lissencephaly after prenatal diagnosis: A case report.

Journal: Medicine

Published: February 17, 2023

DPAGT1-CDG: Recurrent fetal death.

Journal: Birth defects research

Published: January 11, 2023

45, X/ 46, X, psu idic (Y) (q11.2) Mosaicism in a Primary Amenorrhea Girl with Swyer Syndrome.

Journal: Case reports in genetics

Published: November 23, 2022

A fetus with Bosch-Boonstra-Schaaf optic atrophy syndrome characterized by bilateral ventricle widening: A case report and related literature review.

Journal: Medicine

Published: October 12, 2022

Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype.

Journal: Molecular cytogenetics

Published: August 24, 2022