Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference21 articles.
1. Recombinant chromosome 18 resulting from a maternal pericentric inversion
2. Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology
3. Holoprosencephaly: Epidemiologic and clinical characteristics of a California population
4. Abnormal Chromosome 18 in prenatal diagnosis with holoprosencephaly
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1. The molecular mechanisms of recombinant chromosome 18 with parental pericentric inversions and a review of the literature;Journal of Human Genetics;2023-05-10
2. Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies;Taiwanese Journal of Obstetrics and Gynecology;2019-05
3. Cytogenetic, Molecular, and Phenotypic Characterization of a Patient with de novo Derivative Chromosome 18 and Review of the Literature;Cytogenetic and Genome Research;2019
4. A Peruvian Child with 18p-/18q+ Syndrome and Persistent Microscopic Hematuria;Journal of Pediatric Genetics;2017-07-06
5. Del(18p) Syndrome;Atlas of Genetic Diagnosis and Counseling;2017
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