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ALG6
Yeast Genome Gazetteer P35-65
Congenital Disorders of Glycosylation from a Neurological Perspective
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Molecular Diagnostic Requisition
ALG6-CDG in South Africa: Genotype-Phenotype Description of Five Novel Patients
Viruses Like Sugars: How to Assess Glycan Involvement in Viral Attachment
Prenatal Testing Requisition Form
Genetic Predisposition to Fetal Alcohol Syndrome: Association with Congenital Disorders of N-Glycosylation
(F304S) Substitution in the Human ALG6 Gene Is a Common Polymorphism and Not a Causal Mutation of CDG-Ic
F04b57ca351b0dc3389ebe992c
Mutations in PHKA1, PHKG1 Or Six Other Candidate Genes Explain Only a Minority of Cases
Genome-Wide Investigation of Cellular Functions for Trna Nucleus
N-Glycosylation Processing Pathways Across Kingdoms Cheng-Yu Chung, Natalia I
Downregulation of Carnitine Acyl-Carnitine Translocase by Mirnas
Structural and Biochemical Insights Into Biosynthesis and Degradation of and Degradation Into Insights Biosynthesis and Biochemical Structural
SSIEM Classification of Inborn Errors of Metabolism 2011
The Skeletal Manifestations of Deranged Glycosylation
Endocrine Manifestations Related to Inherited Metabolic Diseases in Adults
Top View
Bioinformatics-Based Prediction of FUT8 As a Therapeutic Target in Estrogen Receptor-Positive Breast Cancer Fateme Shaabanpour Aghamaleki1, Shirin Farivar1,*
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Supplemental Figures 04 12 2017
Blueprint Genetics Congenital Disorders of Glycosylation Panel
ALG6-Congenital Disorder of Glycosylation
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Enabling Tools for Toxoplasma Glycobiology 02Sept2018
Congenital Disorders of Glycosylation
Supplementary Table S1. Distributions of Characteristics of CM Patients in MDACC and NHS/HPFS Datasets Parameter Frequency MFT H
Targeted Genes and Methodology Details for Congenital Disorders of Glycosylation Gene Panel
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
Congenital Disorders of Glycosylation
Proteasome Inhibition Supplemental Tables 3 and 4 JO2.Xlsx
Fatal Congenital Heart Glycogenosis Caused by a Recurrent Activating
Hereditary Disorders of Carbohydrate Metabolism
Are Shown B Gene Numbera
The Clinical Relevance of Glycobiology