Recombinant Chromosomes Resulting From Parental Pericentric Inversions—Two New Cases and a Review of the Literature
Author:
Publisher
Frontiers Media SA
Subject
Genetics (clinical),Genetics,Molecular Medicine
Reference27 articles.
1. Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm;Ashley;Mol. Hum. Reprod.,2007
2. Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis;Bhatt;Cytogenet. Genome Res.,2014
3. Novel unbalanced translocations affecting the long arms of Chromosomes 10 and 22 cause complex syndromes with very severe neurodevelopmental delay, speech impairment, autistic behavior, and epilepsy;Coci;Cytogenet. Genome Res.,2017
4. Structural differences in pericentric inversions. Application to a model of risk of recombinants;Daniel;Hum. Genet.,1981
5. Triploidy with complementary recombinant 7s from a paternal inversion 7;Ekblom;Birth Defects Orig. Artic. Ser.,1993
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1. Molecular Cytogenetic Characterization of Rare but Repeatedly Observed Inversions in German Population;Cytogenetic and Genome Research;2024-05-24
2. The molecular mechanisms of recombinant chromosome 18 with parental pericentric inversions and a review of the literature;Journal of Human Genetics;2023-05-10
3. Chromosomal aberrations in patients with suspected Prader Willi syndrome;Salud, Ciencia y Tecnología - Serie de Conferencias;2023-05-08
4. Dicentric Recombinant Chromosome 18 due to Maternal Paracentric Inversion Analyzed by Array CGH;Molecular Syndromology;2023
5. The Precise Breakpoint Mapping in Paracentric Inversion 10q22.2q23.3 by Comprehensive Cytogenomic Analysis, Multicolor Banding, and Single-Copy Chromosome Sequencing;Biomedicines;2022-12-14
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