Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion
Author:
Affiliation:
1. Meram Medical Faculty, Department of Medical Genetics; Necmettin Erbakan University; Konya Turkey
2. Meram Medical Faculty, Medical Biology; Necmettin Erbakan University; Konya Turkey
3. Intergen Genetics Center; Ankara Turkey
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference31 articles.
1. Recombinant chromosome 18 in two offspring of a chromosome 18 inversion heterozygote;Andrews;Ann Genet,1982
2. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3);Asano;Jinrui Idengaku Zasshi,1991
3. Recombinant chromosome 18 resulting from a maternal pericentric inversion;Ayukawa;Am J Med Genet,1994
4. Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18;Boghosian-Sell;Am J Hum Genet,1994
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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. Cytogenetic, Molecular, and Phenotypic Characterization of a Patient with de novo Derivative Chromosome 18 and Review of the Literature;Cytogenetic and Genome Research;2019
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4. A Peruvian Child with 18p-/18q+ Syndrome and Persistent Microscopic Hematuria;Journal of Pediatric Genetics;2017-07-06
5. 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;American Journal of Medical Genetics Part A;2016-09-15
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