Medical dictionary. 2011.
FMR1 — [ thumb|280px|Location of FMR1 on the X chromosome. ] FMR1 (fragile X mental retardation 1) is a human gene that codes for a protein called fragile X mental retardation protein , or FMRP. This protein is normally made in many tissues, especially… … Wikipedia
FMR1 — Das Fragile X Mental Retardation 1 (FMR1; Fragile X Mental Retardation 1) ist ein Gen. Sein Produkt ist das Fragile X Mental Retardation Protein (FMRP). Dabei handelt es sich um ein selektiv RNA bindendes Protein, das im adulten Organismus… … Deutsch Wikipedia
FMR1 gene — [fragile X mental retardation 1] a gene expressed in human brain and testes cells and associated with fragile X syndrome (q.v.) … Medical dictionary
Fragiles X-Syndrom — Klassifikation nach ICD 10 Q99.2 Fragiles X Chromosom Syndrom des fragilen X Chromosoms … Deutsch Wikipedia
Marker-X-Syndrom — Klassifikation nach ICD 10 Q99.2 Fragiles X Chromosom Syndrom des fragilen X Chromosoms … Deutsch Wikipedia
Martin-Bell-Syndrom — Klassifikation nach ICD 10 Q99.2 Fragiles X Chromosom Syndrom des fragilen X Chromosoms … Deutsch Wikipedia
Fragiles-X-Syndrom — Klassifikation nach ICD 10 Q99.2 Fragiles X Chromosom Syndrom des fragilen X Chromosoms … Deutsch Wikipedia
Fragile X syndrome — Classification and external resources Location of FMR1 gene ICD 10 Q99.2 … Wikipedia
Síndrome X frágil — Localización del gen FMR 1. Clasificación y recursos externos CIE 10 Q … Wikipedia Español
Fragile X syndrome — One of the most common causes of inherited mental retardation and neuropsychiatric disease in human beings, affects as many as one in 2000 males and one in 4000 females. The syndrome is also known as FRAXA (the fragile X chromosome itself) and as … Medical dictionary
