- snRPN
- small nuclear ribonucleoprotein polypeptide N
Medical dictionary. 2011.
Medical dictionary. 2011.
SNRPN upstream reading frame protein — SNRPN upstream reading frame, also known as SNURF, is a human gene.cite web | title = Entrez Gene: SNURF SNRPN upstream reading frame| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=8926| accessdate = ] PBB … Wikipedia
snRPN — • small nuclear ribonucleoprotein polypeptide N … Dictionary of medical acronyms & abbreviations
Small nuclear ribonucleoprotein polypeptide N — Small nuclear ribonucleoprotein polypeptide N, also known as SNRPN, is a human gene.cite web | title = Entrez Gene: SNRPN small nuclear ribonucleoprotein polypeptide N| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
PAR1 (gene) — Prader Willi/Angelman region 1 Identifiers Symbols PAR1; D15S227E External IDs OMIM … Wikipedia
Angelman syndrome — Infobox Disease Name = Angelman Syndrome Caption = DiseasesDB = 712 ICD10 = ICD10|Q|93|5|q|90 ICD9 = ICD9|759.89 ICDO = OMIM = 105830 MeshID = D017204 Angelman syndrome (AS) is a neuro genetic disorder characterized by intellectual and… … Wikipedia
Prader-Willi syndrome — Infobox Disease Name = Prader Willi syndrome Caption = DiseasesDB = 10481 ICD10 = ICD10|Q|87|1|q|80 ICD9 = ICD9|759.81 ICDO = OMIM = 176270 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 1880 MeshID = D011218 Prader Willi syndrome… … Wikipedia
Small Nucleolar RNA SNORD64 — SNORD64 (also known as HBII 13) is a non coding RNA (ncRNA) molecule which functions in the biogenesis (modification) of other small nuclear RNAs (snRNAs). This type of modifiying RNA is located in the nucleolus of the eukaryotic cell which is a… … Wikipedia
SNRPB — Small nuclear ribonucleoprotein polypeptides B and B1, also known as SNRPB, is a human gene.cite web | title = Entrez Gene: SNRPB small nuclear ribonucleoprotein polypeptides B and B1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
Prader-Willi-Syndrom — Klassifikation nach ICD 10 Q87.1 Angeborene Fehlbildungssyndrome, die vorwiegend mit Kleinwuchs einhergehen (inkl.: Prader Willi Syndrom) … Deutsch Wikipedia
Síndrome de Prader-Willi — Este artículo o sección tiene un estilo difícil de entender para los lectores interesados en el tema. Si puedes, por favor edítalo y contribuye a hacerlo más accesible para el público general, sin eliminar los detalles técnicos que interesan a… … Wikipedia Español