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C16orf82
Autism Multiplex Family with 16P11.2P12.2 Microduplication Syndrome in Monozygotic Twins and Distal 16P11.2 Deletion in Their Brother
Copy Number Variation in Fetal Alcohol Spectrum Disorder
Looking for Missing Proteins in the Proteome Of
A Genome-Wide Association Study Confirming a Strong Effect of HLA and Identifying Variants in CSAD/Lnc-ITGB7-1 on Chromosome
Genome- Wide Association Studies of 52 Cognitive Phenotypes
Us 2018 / 0305689 A1
Non-Syndromic Cleft Lip with Or Without Cleft Palate
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
A Point of Rarity in Genetic Risk for Bipolar Disorder and Schizophrenia
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Integrated Analysis of Differentially Expressed Genes and Construction
Genetic Susceptibility to Periodontal Disease in Down Syndrome: a Case-Control Study
Identifying Transcriptomic Correlates of Histology Using Deep Learning
Key Genes Associated with Diabetes Mellitus and Hepatocellular Carcinoma T ⁎ ⁎ Gao-Min Liu , Hua-Dong Zeng, Cai-Yun Zhang, Ji-Wei Xu
Suppementary Table 9. Predicted Targets of Hsa-Mir-181A by Targetscan 6.2
Expression Quantitative Trait Loci As Possible Biomarkers on Depression: Candidate Gene and Genome-Wide Approaches
WO 2010/074924 Al
Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder
Top View
SUPPLEMENTARY INFORMATION Doi:10.1038/Nature18299
Identifying Genetic Variation Contributing to Keratoconus
Product Data Sheet
For Peer Review Only - BMJ Open: First Published As 10.1136/Bmjopen-2014-006920 on 6 May 2015