RBM15
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MKL1 — Megakaryoblastic leukemia (translocation) 1, also known as MKL1, is a human gene.cite web | title = Entrez Gene: MKL1 megakaryoblastic leukemia (translocation) 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
Down syndrome — Classification and external resources Boy with Down syndrome assembling a … Wikipedia
XYY syndrome — Not to be confused with XXY (2 X s, Klinefelter s syndrome). XYY syndrome Classification and external resources Y chromosome ICD 10 Q … Wikipedia
Fragile X syndrome — Classification and external resources Location of FMR1 gene ICD 10 Q99.2 … Wikipedia
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
Multiple myeloma — Classification and external resources Micrograph of a plasmacytoma, the histologic correlate of multiple myeloma. H E stain ICD … Wikipedia
Aneuploidy — Classification and external resources ICD 10 Q90 Q98 ICD 9 … Wikipedia
Patau syndrome — Classification and external resources Chromosome 13 ICD 10 Q91.4 Q … Wikipedia
Nondisjunction — ( not coming apart ) is the failure of chromosome pairs to separate properly during meiosis stage 1 or stage 2. This could arise from a failure of homologous chromosomes to separate in meiosis I, or the failure of sister chromatids to separate… … Wikipedia
Chromosomal translocation — of the 4th and 20th chromosome. In genetics, a chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes. A gene fusion may be created when the translocation joins two otherwise… … Wikipedia