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1. Xp11.2 duplication: Xp11.2 duplication is a genomic variation marked by the duplication of an X chromosome region on the short arm p at position 11.2, defined by standard karyotyping (G-banding). This gene-rich, rearrangement prone region can be further ... (Medicine) [100%] 2023-12-24 [Genetic diseases and disorders]
2. Segmental duplication: Segmental duplications (SDs) are segments of DNA with near-identical sequences. Segmental duplications, also known as low copy repeats (LCRs), are believed to have played a role in creating new primate genes as reflected in human genetic variation. (Biology) [100%] 2023-06-30 [Molecular genetics] [Mutation]...
3. Gene duplication: Gene duplication is the insertion of the same gene into different parts of the genome of an organism. This typically occurs as the result of copying errors during cell division, though it can also occur if an existing gene is ... [100%] 2023-07-15
4. Caudal duplication: Caudal duplication, (or caudal duplication syndrome) is a rare congenital disorder in which various structures of the caudal region, embryonic cloaca, and neural tube exhibit a spectrum of abnormalities such as duplication and malformations. The exact causes of the condition ... (Medicine) [100%] 2023-09-30 [Congenital disorders]
5. 8p23.1 duplication syndrome: 8p23.1 duplication syndrome is a rare genetic disorder caused by a duplication of a region from human chromosome 8. This duplication syndrome has an estimated prevalence of 1 in 64,000 births and is the reciprocal of the 8p23 ... (Medicine) [81%] 2023-12-30 [Syndromes affecting the heart]
6. Partial 9p duplication: Articles Most recent articles on Partial 9p duplication Most cited articles on Partial 9p duplication Review articles on Partial 9p duplication Articles on Partial 9p duplication in N Eng J Med, Lancet, BMJ Media Powerpoint slides on Partial 9p duplication ... [81%] 2023-08-06 [Disease]
7. 7q11.23 duplication syndrome: 7q11.23 duplication syndrome (also called dup7 or Duplication of the Williams-Beuren Syndrome Critical Region) is a rare genetic syndrome caused by micro-duplication of 1.5-1.8 mega base in section q11.23 of chromosome 7. This ... (Medicine) [81%] 2023-09-15
8. MECP2 duplication syndrome: MECP2 duplication syndrome (M2DS) is a rare disease that is characterized by severe intellectual disability and impaired motor function. It is an X-linked genetic disorder caused by the overexpression of MeCP2 protein. (Medicine) [81%] 2023-09-13 [Gene expression] [Disorders causing seizures]...
9. 1q21.1 duplication syndrome: 1q21.1 duplication syndrome or 1q21.1 (recurrent) microduplication is a rare aberration of chromosome 1. On chromosome 1, a human cell typically has one pair of identical chromosomes. (Medicine) [81%] 2023-11-25 [Syndromes affecting the nervous system]
10. MECP2 duplication syndrome: MECP2 duplication syndrome (M2DS) is a rare disease that is characterized by severe intellectual disability and impaired motor function. It is an X-linked genetic disorder caused by the overexpression of MeCP2 protein. [81%] 2023-10-28 [Gene expression] [Chromosome instability syndromes]...
11. 1q21.1 duplication syndrome: 1q21.1 duplication syndrome or 1q21.1 (recurrent) microduplication is a rare aberration of chromosome 1. On chromosome 1, a human cell typically has one pair of identical chromosomes. [81%] 2024-01-01 [Rare genetic syndromes] [Autosomal duplications]...
12. Enteric duplication cyst: Enteric duplication cysts, sometimes simply called duplication cysts, are rare congenital malformations of the gastrointestinal tract. They most frequently occur in the small intestine, particularly the ileum, but can occur anywhere along the gastrointestinal tract. [81%] 2023-10-27 [Congenital disorders of digestive system]
13. MECP2 duplication syndrome: MECP2 duplication syndrome (M2DS) is a rare disease that is characterized by severe intellectual disability and impaired motor function. It is an X-linked genetic disorder caused by the overexpression of MeCP2 protein. [81%] 2024-03-05 [Gene expression] [Chromosome instability syndromes]...
14. 1q21.1 duplication syndrome: 1q21.1 duplication syndrome, also known as 1q21.1 microduplication, is an uncommon copy number variant associated with several congenital abnormalities, including developmental delay, dysmorphic traits, autism spectrum disorder, and congenital cardiac defects. Common facial features include frontal bossing, hypertelorism ... [81%] 2024-07-15 [Rare genetic syndromes] [Autosomal duplications]...
15. Duplication of the cube: The problem of constructing a cube having twice the volume of a given cube; it is one of the classical problems of Antiquity, to find an exact construction with ruler and compass. If an edge of the given cube has ... (Mathematics) [70%] 2023-09-23
16. FM Non-Duplication Rule: The FM Non-Duplication Rule was adopted by the U.S. Federal Communications Commission (FCC) on July 1, 1964, after a year's consideration. (U.S. government regulation requiring 50% original content on FM radio stations) [70%] 2023-05-30 [Broadcast law] [History of radio]...
17. Duplication and elimination matrices: In mathematics, especially in linear algebra and matrix theory, the duplication matrix and the elimination matrix are linear transformations used for transforming half-vectorizations of matrices into vectorizations or (respectively) vice versa. The duplication matrix \displaystyle{ D_n }[/math] is the ... [70%] 2023-08-20 [Matrices]
18. Chromosome 2q31.1 duplication syndrome gene: Chromosome 2q31.1 duplication syndrome is a protein that in humans is encoded by the DUP2Q31.1 gene. (Genetic element in the species Homo sapiens) [63%] 2022-10-31
19. Segmental Duplication on the Human Y Chromosome: Segmental duplication are blocks of DNA ranging from 1 to 400kb in length which recur at multiple sites within the genome, sharing greater than 90% similarity. Multiple studies have found a correlation between the location of segmental duplications and regions ... [53%] 2024-01-09 [Chromosomes (human)] [DNA]...
20. G-Protein Coupled Receptor Gene Duplication Project: The broad aim of this project is to analyze genomic sequence data with hidden Markov models (HMMs). The HMM analysis program used is called HMMER and can be downloaded here. [53%] 2024-01-05