Prenatal diagnosis and molecular cytogenetic characterization of hereditary chromosomal deletions and duplications with a favorable outcome
Main Authors: | Guoqiang Sun, Lijuan Han, Shuxin Hu, Xu Liu, Bo Wang |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2021-09-01
|
Series: | Taiwanese Journal of Obstetrics & Gynecology |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1028455921002047 |
Similar Items
-
Prenatal diagnosis and molecular cytogenetic characterization of two hereditary chromosomal duplications with favorable outcomes
by: Y.J. Wu, et al.
Published: (2020-10-01) -
Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy
by: Chih-Ping Chen, et al.
Published: (2011-12-01) -
Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication
by: Chih-Ping Chen, et al.
Published: (2020-01-01) -
Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings
by: Chih-Ping Chen, et al.
Published: (2010-12-01) -
Prenatal detection and molecular cytogenetic characterization of Xp deletion and Xq duplication: a case report and literature review
by: Qing Lin, et al.
Published: (2024-02-01)