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  1. ..., Eisfeldt J, Du H, Bertola DR, Oliveira D, Costa SS, Lupski JR, Lindstrand A, Carvalho CMB. 2021. Chromoanagenesis event underlies a de novo pericentric and multiple paracentric inversions in a single chromosome causing Coffin-Siris syndrome. Front Genet 12: 708348. doi:10.3389/fgene.2021.708348 ↵Grochowski...
  2. ...recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16. Genome Res 15: 1232–1242. Grimwood J, Gordon LA, Olsen A, Terry A, Schmutz J, Lamerdin J, Hellsten U, Goodstein D, Couronne O, Tran-Gyamfi M, et al. 2004. The DNA sequence...
  3. ...2001 ). More recently, nonallelic homologous recombination between such sequences has been postulated to underlie evolutionary chromosome rearrangements ( Tunnacliffe et al. 1993 ; Nickerson et al. 1999 ; Valero et al. 2000 ; Dehal et al. 2001 ; Stankiewicz et al. 2001 ). To more specifically test...
  4. ...to be isosequential. A pericentric inversion differentiated the gorilla ( Gorilla gorilla , GGO) chromosome 18 (phylogenetic XIV, data not shown) consistent with previous analyses using banding techniques ( Yunis and Prakash 1982 ). Marker order of phylogenetic chromosome XV was found to be collinear in HSA, GGO...
  5. ...be unambiguously resolved because of recent pericentric inversion. (***) Three distinct hybridization signals could be distinguished on GGO chromosome 17q11 (HSA 16p11 equivalent). ( c ) Comparative FISH analysis of CAGGG repeat probe, 196.3.12. Representative hybridizations of chromosomal metaphases are shown...
  6. .... A catalog of such lineage-specific genes provides a roadmap for the identification of genes important for recent innovations in immunity, drug detoxification, and reproduction ( Copley et al. 2003 ). Third, at a structural level, regions of highly homologous duplications are preferential sites of inversion...
  7. ...well known common chromosomal polymorphisms (e.g., inversion on chromosome 9; de la Chapelle et al. 1974 ; Lee 2005 ), the aber ration is assumed to be the cause of the clinically recognized abnormal phenotype. View this table: In this window In a new window Table 3. Examples of disorders caused...
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