In genetics, a deletion (also called gene deletion, deficiency, or deletion mutation) (sign: Δ) is a mutation (a genetic aberration) in which a part of...

22q13 deletion syndrome, known as Phelan–McDermid syndrome (PMS), is a genetic disorder caused by deletions or rearrangements on the q terminal end (long...

Storm, 2016 Deletion (genetics), deletion of a gene or chromosome segment, symbolized in the literature by a Δ symbol Elision, the deletion of a sound...

19 September 2018. "1p36 deletion syndrome". Genetics Home Reference. NIH. Battaglia, Agatino (June 6, 2013). "1p36 Deletion Syndrome – RETIRED CHAPTER...

Aneuploidy Antioxidant Behavior mutation Budgerigar colour genetics DbDNV (2010) Deletion (genetics) Ecogenetics Embryology Homeobox Human somatic variation...

Wolf–Hirschhorn syndrome (WHS) is a chromosomal deletion syndrome resulting from a partial deletion on the short arm of chromosome 4 [del(4)(p16.3)]....

disorder resulting from deletion of genes from chromosome 11 that includes band 11q24.1. It is a congenital disorder. Since the deletion takes place on the...

DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22. While the symptoms...

deletion syndrome is a rare aberration of chromosome 1. A human cell has one pair of identical chromosomes on chromosome 1. With the 1q21.1 deletion syndrome...

9q34 deletion syndrome is a rare genetic disorder. Terminal deletions of chromosome 9q34 have been associated with childhood hypotonia, a distinctive facial...

copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis". Human Molecular Genetics. 9 (4): 489–501. doi:10.1093/hmg/9...

Roberts, Timothy PL; et al. (1 June 2021). "16p11.2 deletion syndrome". Current Opinion in Genetics & Development. 68: 49–56. doi:10.1016/j.gde.2021.01...

births Chromosome 15q trisomy Genetics Genetic deletion "Chromosome15q deletion". nih.gov. Retrieved 2016-08-05. "15q deletion" (PDF). rarechromo.org. Archived...

Chromosomal deletion syndromes result from deletion of parts of chromosomes. Depending on the location, size, and whom the deletion is inherited from...

mutagenesis Loss-of-Function Mutations Gain-of-Function Mutations Deletion (genetics) Banavali, Nilesh K. (2013). "Partial Base Flipping is Sufficient...

recent development of the FISH for 17p11.2 deletion test has allowed more accurate detection of this deletion. However, further testing is required for...

Genetics is the study of genes, genetic variation, and heredity in organisms. It is an important branch in biology because heredity is vital to organisms'...

deletion syndrome is a rare genetic disorder caused by the deletion of small fragments of chromosome 3. Reports symptoms in patients with 3p deletion...

qter". Human Genetics. 47 (3): 233–237. doi:10.1007/BF00321014. PMID 457112. S2CID 32976833. "10q26 deletion syndrome: MedlinePlus Genetics". MedlinePlus...

whereas longer in-frame indels were rare outcomes. Insertion (genetics) Deletion (genetics) Mahmoud, Medhat; Gobet, Nastassia; Cruz-Dávalos, Diana Ivette;...

cells of multicellular animals Interstitial deletion and duplication in genetics, see deletion (genetics)#Types and gene duplication Interstitial granulomatous...

du chat syndrome is a rare genetic disorder due to a partial chromosome deletion on chromosome 5. Its name is a French term ("cat-cry" or "call of the cat")...

2q37 deletion syndrome is a disorder caused by the deletion of a small piece of chromosome 2 in which one or more of 3 sub-bands, 2q37.1, 2q37.2, and 2q37...

aneuploidy, chromosomal rearrangements, and genomic deletion/duplication disorders. Molecular genetics involves the discovery of and laboratory testing for...

(June 2014). "The Yeast Deletion Collection: A Decade of Functional Genomics". Genetics. 197 (2): 451–465. doi:10.1534/genetics.114.161620. ISSN 0016-6731...

coloration, 'salmiak,' is associated with a 95-kb deletion downstream of the KIT gene". Animal Genetics. doi:10.1111/age.13438. ISSN 0268-9146. Lyons, L...

this study it is suggested on a growing basis of evidence, that not only genetics but also epigenetics, contribute to aneuploid cell formation. The terms...

of Medical Genetics. 42 (4): 318–21. doi:10.1136/jmg.2004.024646. PMC 1736032. PMID 15805158. Bearden C (2016-10-18). "Same DNA deletion paves paths...

microdeletion syndrome, also known as 17q12 deletion syndrome, is a rare chromosomal anomaly caused by the deletion of a small amount of material from a region...

imprinted gene in the Prader-Willi deletion region, which is highly expressed in brain". American Journal of Human Genetics. 67 (5): 1067–82. doi:10.1086/303106...