- USH2A
- Usher syndrome type IIA
Medical dictionary. 2011.
USH2A
Look at other dictionaries:
USH2A — Usher syndrome 2A (autosomal recessive, mild), also known as USH2A, is a human gene. PBB Summary section title = summary text = This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs … Wikipedia
USH2A — • Usher syndrome type IIA … Dictionary of medical acronyms & abbreviations
Usher syndrome — Classification and external resources OMIM 276900 276901 DiseasesDB 13611 … Wikipedia
Usherina — Símbolo USH2A Símbolos alt. US2; USH2; dJ1111A8.1 Datos genéticos Código de gen USH2A … Wikipedia Español
Síndrome de Usher — Clasificación y recursos externos OMIM 276900 … Wikipedia Español
Usher-Syndrom — Klassifikation nach ICD 10 Q87.8 Usher Syndrom H35.5 Hereditäre Netzhautdystrophie H90.3 … Deutsch Wikipedia
Usher Syndrom — Klassifikation nach ICD 10 Q87.8 Usher Syndrom H35.5 Hereditäre Netzhautdystrophie … Deutsch Wikipedia
1-я хромосома человека — Идиограмма 1 й хромосомы человека 1 я хромосома человека самая большая из 23 человеческих хромосом, одна из 22 аутосом человека. Хромосома содержит около 248 млн пар оснований … Википедия
Chromosome 1 (human) — Map of Chromosome 1 Chromosome 1 is the designation for the largest human chromosome. Humans have two copies of chromosome 1, as they do with all of the autosomes, which are the non sex chromosomes. Chromosome 1 spans about 247 million nucleotide … Wikipedia
USH1C — Usher syndrome 1C (autosomal recessive, severe), also known as USH1C, is a human gene. [cite web | title = Entrez Gene: USH1C Usher syndrome 1C (autosomal recessive, severe)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
