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*  Ancestral reconstruction
Watterson, G.A.; Ewens, W.J.; Hall, T.E.; Morgan, A. (1982). "The chromosome inversion problem". Journal of Theoretical Biology ... Sturtevant, A. H.; Dobzhansky, T. (1936). "Inversions in the Third Chromosome of Wild Races of Drosophila Pseudoobscura, and ... Dobzhansky, Theodosius; Sturtevant, Alfred (1938). "Inversions in the chromosomes of Drosophila pseudoobscura". Genetics. 23 (1 ... Various operations are allowed on these permutations, such as an inversion (a segment of the permutation is reversed in-place ...
*  Alfred Sturtevant
Chromosome Map. NCBI. April 11, 2007 gi?rid=gnd.chapter.272 Definition of Chromosome Inversion. April 11, 2007. http://www. ... Lattas, Chelsea K. Chromosome Inversions. Michigan State University. April 11, 2007 < http://www.msu.edu/~lattasch/inversion. ... This was the beginning of the chromosome theory; Roux viewed his findings as argument that chromosomes contain units of ... In 1913, he determined that genes were arranged on chromosomes in a linear fashion, like beads on a necklace. He also showed ...
*  Rabicano
brooks, SA; TL Lear; DL Adelson; E Bailey (2007). "A chromosome inversion near the KIT gene and the Tobiano spotting pattern in ...
*  Fraser syndrome
An earlier born infant had Fraser syndrome and the same chromosome 9 inversion. Van Haelst et al. (2007) provided a revision of ... 2003) located the Fraser syndrome locus to chromosome 4q21. Genetic Heterogeneity In 6 of 18 consanguineous families with ... Both the female fetus and the phenotypically normal father had a chromosome anomaly: inv(9)(p11q21). ...
*  Acute basophilic leukemia
Liu, P.P.; A. Hajara; C. Wijmengac; F.S. Collins (1995). "Molecular pathogenesis of chromosome 16 inversion in the M4E0 ... Cytogenetically heterogeneous but frequently associated with Philadelphia chromosome. There is no clinically distinguishing ...
*  Stickleback
Some variants, and several chromosome inversions, consistently distinguish marine and freshwater populations, helping identify ...
*  AI-10-49
The pericentric chromosome inversion inv(16)(p13q22) creates the CBFB-MYH11 fusion gene, which encodes the CBFβ-SMMHC fusion ... including groups with the chromosome rearrangements inv(16)(p13q22) and t(8;21)(q22;q22). The chromosome translocation t(8;21)( ... The chromosome translocation t(12;21) (p13.1;q22) causes the fusion of the ETS variant 6 (ETV6) and RUNX1 genes results in ETV6 ... The RUNX1 and CBFB genes are targets of chromosome rearrangements that create oncogenic fusion genes in leukemia. ...
*  Roan (horse)
Haase, B; Jude R; Brooks SA; Leeb T (June 2008). "An equine chromosome 3 inversion is associated with the tobiano spotting ... The region of the chromosome that harbors the roan gene is homologous to parts of chromosomes in other species that also ... grandpa's chromosome 8, but a mixture of DNA from each parent. Instead, paired chromosomes exchange parallel pieces of DNA, a ... While a chromosomal inversion of KIT causes tobiano white spotting, KIT also harbors one or more alleles responsible for sabino ...
*  Underdominance
Project Population Genetics The Stability of An Equilibrium and the Average Fitness of a Population Chromosome Inversions, ... In this model, two genetics constructs are introduced into two non-homologous chromosomes. Each construct is lethal when ...
*  Chromosomal inversion
An inversion is a chromosome rearrangement in which a segment of a chromosome is reversed end to end. An inversion occurs when ... The most common inversion seen in humans is on chromosome 9, at inv(9)(p12q13). This inversion is generally considered to have ... Paracentric inversions do not include the centromere and both breaks occur in one arm of the chromosome. Pericentric inversions ... Gardner, R.J.M; Sutherland, Grant R.; Shaffer, Lisa G. (2011). "9 Inversions". Chromosome Abnormalities and Genetic Counseling ...
*  Benign familial neonatal seizures
This occurs on chromosome 5 and the inversion is of the p15 through q11 area. Affected individuals, thus, have the karyotype 46 ... "Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions". J Med Genet. 39 (3): 214-6. doi: ... The rarest cause of BFNE, occurring in only one known family, is a chromosomal inversion. ... and the third being a chromosomal inversion (BFNC3). There is no obvious correlation between most of the known mutations and ...
*  TMEM200A
"Candidate psychiatric illness genes identified in patients with pericentric inversions of chromosome 18". Psychiatric Genetics ...
*  Biopsychiatry controversy
March 2005). "Candidate psychiatric illness genes identified in patients with pericentric inversions of chromosome 18". ... December 2004). "A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42". ...
*  Michelin tire baby syndrome
A child with multiple anomalies, smooth muscle hamartoma, and familial paracentric inversion of chromosome 7q". J Am Acad ...
*  T-cell prolymphocytic leukemia
The most frequent chromosomal abnormality is the inversion of chromosome 14, specifically inv 14(q11;q32). This is found in 80 ... Brito-Babapulle V, Catovsky D (1991). "Inversions and tandem translocations involving chromosome 14q11 and 14q32 in T- ... Maljaei SH, Brito-Babapulle V, Hiorns LR, Catovsky D (1998). "Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic ... abnormalities of chromosome 8 are seen approximately 75% of patients, including idic (8p11), t(8;8)(p11-12;q12), and trisomy 8 ...
*  22q13 deletion syndrome
"A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome". ... That observation lead to an emphasis on the SHANK3 gene, which resides close to the terminal end of chromosome 22. Interest in ... 2013). "Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion". Am ... the paternal chromosome in 75% of cases), from 22q13.3 to 22qter. Although the deletion is most typically a result of a de novo ...
*  DUF1220
This in turn may have mediated the HLS pericentric inversion on chromosome 1, an important evolutionary event. For the above ... In the human genome DUF1220 sequences are located primarily on chromosome 1 in region 1q21.1-q21.2, with several copies also ... Improved characterization of the genomic architecture of chromosome 1 in a new genomic assembly has allowed for more refined ... "Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes". N. Engl. J. Med. 359 (16): 1685-99. doi: ...
*  Rearrangement
Translocations Ring chromosomes Chromosomal inversions. ...
*  End-sequence profiling
Chromosome abnormalities Chromosomal inversion Insertion (genetics) Deletion (genetics) Chromosomal translocation Chromosome ... The classic strategy to construct an artificial chromosome is bacterial artificial chromosome (BAC). Basically, the target ... the fragments is cloned into plasmids to construct artificial chromosome such as bacterial artificial chromosomes (BAC) which ... Inversion can be detected by divergent orientation of the reads, where the insert will have two plus-end or two minus-end. In ...
*  Emerin
Approximately 20% of cases have X chromosomes with an inversion within the Xq28 region. Moreover, recent research have found ... Small K, Warren ST (Jan 1998). "Emerin deletions occurring on both Xq28 inversion backgrounds". Human Molecular Genetics. 7 (1 ... "Transcriptional organization of a 450-kb region of the human X chromosome in Xq28". Proc. Natl. Acad. Sci. U.S.A. 90 (23): ...
*  PEX1
... report of the second case associated with a pericentric inversion of chromosome 7". Hum. Genet. 84 (1): 79-80. doi:10.1007/ ... 2003). "Human chromosome 7: DNA sequence and biology". Science. 300 (5620): 767-72. doi:10.1126/science.1083423. PMC 2882961 . ... 2003). "The DNA sequence of human chromosome 7". Nature. 424 (6945): 157-64. doi:10.1038/nature01782. PMID 12853948. ...
*  Brenden Adams
The condition is caused by an inversion in the 12th chromosome. His activities include joining a middle school football team. ...
*  Chromosome engineering
Genetics Chromosome Chromosomal deletion Chromosomal inversion Chromosomal translocation DNA Disease "Chromosome engineering". ... Chromosome engineering is "the controlled generation of chromosomal deletions, inversions, or translocations with defined ... In an experiment pertaining to chromosome engineering that was conducted in 2006, it was found that chromosome engineering can ... After much experimenting, it was found that manipulating chromosomes, or chromosome engineering, is an excellent and efficient ...
*  ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities
Chromosome inversion in normal individual (Q95.2) Balanced autosomal rearrangement in abnormal individual (Q95.3) Balanced sex/ ... Male with sex chromosome mosaicism (Q98.8) Other specified sex chromosome abnormalities, male phenotype (Q98.9) Sex chromosome ... Chromosome replaced with ring or dicentric (Q93.3) Deletion of short arm of chromosome 4 Wolff-Hirschorn syndrome (Q93.4) ... Deletion of short arm of chromosome 5 Cri-du-chat syndrome (Q93.5) Other deletions of part of a chromosome Angelman syndrome ( ...
*  Chimpanzee genome project
... chromosome segment inversions on human chromosomes 1, 4, 5, 9, 12, 15, 16, 17, and 18. After the completion of the Human genome ... Human and chimpanzee chromosomes are very similar. The primary difference is that humans have one fewer pair of chromosomes ... Humans have 23 pairs of chromosomes and other great apes have 24 pairs of chromosomes. In the human evolutionary lineage, two ... "Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regions". ...