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PCYT1A
Clinical Application of Chromosomal Microarray Analysis for Fetuses With
A Molecular Quantitative Trait Locus Map for Osteoarthritis
Coexpression Networks Based on Natural Variation in Human Gene Expression at Baseline and Under Stress
Data-Driven and Knowledge-Driven Computational Models of Angiogenesis in Application to Peripheral Arterial Disease
The Identification of the High Risk of Metabolic Syndrome by Applying MDR and Jalview Bioinformatics Programs
The Liberfarb Syndrome, a Multisystem Disorder Affecting Eye, Ear, Bone, and Brain Development, Is Caused by a Founder Pathogenic Variant in the PISD Gene
Mutations in PCYT1A, Encoding a Key Regulator of Phosphatidylcholine Metabolism, Cause Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy
Biamino, Elisa; Di Gregorio, Eleonora
Rodrigo Jardim Monteiro Da Fonseca Tese.Pdf
Behavioral Changes and Growth Deficits in a CRISPR Engineered Mouse Model of the Schizophrenia-Associated 3Q29 Deletion
Convergent and Distributed Effects of the 3Q29 Deletion on the Human Neural Transcriptome ✉ Esra Sefik1,2,7, Ryan H
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GWAS Reveals Loci Associated with Velopharyngeal Dysfunction
A Comprehensive Database for Genes and Mutations
Inbreeding and Inbreeding Depression in Linebred Beef Cattle (PDF)
Explaining Rare Mendelian Phenotypes: Exome Sequencing And
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