Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: Prenatal diagnosis and aCGH characterization using uncultured amniocytes
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference58 articles.
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1. The genotype and phenotype of chromosome 18p deletion syndrome;Medicine;2021-05-07
2. Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associations;Prenatal Diagnosis;2020-02-10
3. A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing;Molecular Cytogenetics;2019-12
4. Phenotype to genotype characterization by array-comparative genomic hydridization (a-CGH) in case of fetal malformations: A systematic review;Taiwanese Journal of Obstetrics and Gynecology;2019-01
5. Premaxilla: up to which age it remains separated from the maxilla by a suture, how often it occurs in children and adults, and possible clinical and therapeutic implications: Study of 1,138 human skulls;Dental Press Journal of Orthodontics;2018-12
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