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
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference12 articles.
1. A boy with partial dup (18q)/del (18p) due to a maternal pericentric inversion: genotype–phenotype correlation and risk of recombinant chromosomes based on systematic review of the literature;Lustosa-Mendes;Am J Med Genet,2017
2. Partial deletion of 18p and partial duplication of 18q caused by a paternal pericentric inversion;Israëls;Clin Genet,1996
3. Sperm studies in heterozygote inversion carriers: a review;Anton;Cytogenet Genome Res,2005
4. Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18) dup (18q) inv (18)(p11. 31q11. 2) mat;Leonard;Prenat Diagn,2000
5. Congenital Cystic adenomatoid malformation of the lung coexisting with recombinant chromosome 18;Roberts;Fetal Diagn Ther,2001
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1. Prenatal detection of distal 18p deletion by chromosomal microarray analysis: Three case reports and literature review;Medicine;2024-07-26
2. Prenatal diagnosis of 18p deletion and 8p trisomy syndrome: literature review and report of a novel case;BMC Women's Health;2024-04-15
3. Prenatal Diagnosis of 18p Deletion and 8p Trisomy Syndrome: Case Report and Review of Literature;2023-11-01
4. The molecular mechanisms of recombinant chromosome 18 with parental pericentric inversions and a review of the literature;Journal of Human Genetics;2023-05-10
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