루이스카딘 : 다나와 통합검색

By A Mystery Man Writer
루이스카딘 : 다나와 통합검색
루이스카딘 : 다나와 통합검색

UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCN

루이스카딘 : 다나와 통합검색

UBE4A (NM_004788) Human Untagged Clone - OriGene

루이스카딘 : 다나와 통합검색

OSXApp/venv/lib/python2.7/site-packages/jinja2/_stringdefs.py at master · MultiQC/OSXApp · GitHub

루이스카딘 : 다나와 통합검색

UA845UWB/LC - Antenna Distribution System - Shure Europe

루이스카딘 : 다나와 통합검색

flask-boilerplate/env/Lib/site-packages/jinja2/_stringdefs.py at master · Cpt-SnowCrash/flask-boilerplate · GitHub

루이스카딘 : 다나와 통합검색

PDF] Biallelic UNC80 mutations caused infantile hypotonia with psychomotor retardation and characteristic facies 2 in two Chinese patients with variable phenotypes.

루이스카딘 : 다나와 통합검색

BIS013J

루이스카딘 : 다나와 통합검색

UA845UWB Antenna Distribution System

루이스카딘 : 다나와 통합검색

Index of /Locked/media/ch08

루이스카딘 : 다나와 통합검색

Index of /Locked/media/ch08