- faciogenital
- fa·cio·gen·i·tal (fa″she-o-genґĭ-təl) [facio- + genital] pertaining to or affecting the face and genitalia
Medical dictionary. 2011.
faciogenital
Look at other dictionaries:
faciogenital dysplasia — faciogenital dysplasia. См. синдром Аарскога. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
faciogenital dysplasia — Aarskog syndrome … Medical dictionary
displasia faciogenital — desórden hereditario muy raro ligado al cromosoma X caracterizado por una corta estatura y anormalidades musculares y genitales con retraso mental. Véase: síndrome de AARSKOG Diccionario ilustrado de Términos Médicos.. Alvaro Galiano. 2010 … Diccionario médico
FGDY — faciogenital dysplasia … Medical dictionary
FGDY — • faciogenital dysplasia … Dictionary of medical acronyms & abbreviations
FGD1 (gene) — FYVE, RhoGEF and PH domain containing 1 (faciogenital dysplasia), also known as FGD1, is a human gene.cite web | title = Entrez Gene: FGD1 FYVE, RhoGEF and PH domain containing 1 (faciogenital dysplasia)| url =… … Wikipedia
Aarskog-Scott syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29329 ICD10 = ICD10|Q|87|1|q|80 ICD9 = ICD9|759.89 ICDO = OMIM = 100050 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Aarskog Scott syndrome is an inherited disease characterized by … Wikipedia
Síndrome de Aarskog-Scott — Clasificación y recursos externos CIE 10 Q 87.1; q 80 CIE 9 759.89 OMIM … Wikipedia Español
Drebrin-like — PDB rendering based on 1x67 … Wikipedia
FGD3 — FYVE, RhoGEF and PH domain containing 3, also known as FGD3, is a human gene.cite web | title = Entrez Gene: FGD3 FYVE, RhoGEF and PH domain containing 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
