- interstitial deletion
- loss of a segment within a chromosome arm. See illustration at aberration.
Medical dictionary. 2011.
Medical dictionary. 2011.
Deletion (genetics) — Deletion on a chromosome 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 a chromosome or a sequence of DNA is missing. Deletion is the loss of … Wikipedia
Deletion — Loss of a segment of DNA from a chromosome (and hence from the genome). The first human chromosome deletion was detected in 1963 by Jerome Lejeune and his colleagues in Paris. They discovered loss of part of 5p, the short (p) arm of chromosome 5 … Medical dictionary
Chromosome 5q deletion syndrome — Classification and external resources Photomicrograph of bone marrow showing abnormal mononuclear megakaryocytes typical of 5q syndrome ICD O: M … Wikipedia
Smith–Magenis syndrome — Classification and external resources ICD 9 758.33 OMIM 182290 DiseasesDB … Wikipedia
Smith-Magenis syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 31737 ICD10 = ICD9 = ICD9|758.33 ICDO = OMIM = 182290 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Smith Magenis Syndrome (SMS) is a developmental disorder that affects many parts… … Wikipedia
Gap-43 protein — Growth associated protein 43 Identifiers Symbols GAP43; B 50; PP46 External IDs OMIM … Wikipedia
Glypican 3 — Glypican 3, also known as GPC3, is a human gene.cite web | title = Entrez Gene: GPC3 glypican 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=2719| accessdate = ] cite journal | author = Jakubovic BD,… … Wikipedia
Adenosine deaminase — (also known as ADA) is an enzyme (EC number|3.5.4.4) involved in purine metabolism. It is needed for the breakdown of adenosine from food and for the turnover of nucleic acids in tissues.ReactionsADA irreversibly deaminates adenosine, converting… … Wikipedia
RPE (gene) — Ribulose 5 phosphate 3 epimerase, also known as RPE, is a human gene.cite web | title = Entrez Gene: RPE ribulose 5 phosphate 3 epimerase| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=6120| accessdate = ] … Wikipedia
WAGR syndrome — Wilms tumour (see nephroblastoma), aniridia, genitourinary abnormalities, and mental retardation: a condition due to a deletion of part of the short arm of chromosome 11. * * * a syndrome of Wilms tumor, aniridia, genitourinary abnormalities or… … Medical dictionary