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VCX
Microduplication of Xp22.31 and MECP2 Pathogenic Variant in a Girl with Rett Syndrome: a Case Report
OTX2 Homeoprotein Functions in Adult Choroid Plexus
Identification of Novel Genes for X-Linked Mental Retardation
A Transcriptional Signature of Postmitotic Maintenance in Neural Tissues
Abstracts from the 51St European Society of Human Genetics Conference: Electronic Posters
Copy Number Gain of VCX, X-Linked Multi-Copy Gene, Leads to Cell Proliferation and Apoptosis During Spermatogenesis
Sequence Analysis in Bos Taurus Reveals Pervasiveness of X–Y Arms Races in Mammalian Lineages
Characterizing Genomic Duplication in Autism Spectrum Disorder by Edward James Higginbotham a Thesis Submitted in Conformity
An Isolated TCR Αβ Restricted by HLA-A*02:01/CT37 Peptide Redirecting
VCX3A Polyclonal Antibody (A01) Once in Y-Linked Members
PDZD7-MYO7A Complex Identified in Enriched Stereocilia Membranes
Whole Exome Sequencing in Recurrent Early Pregnancy Loss
Sex-Specific Selection on the Human X Chromosome?
The Origin and Evolution of Human Ampliconic Gene Families and Ampliconic Structure
VCX (NM 013452) Human Mass Spec Standard Product Data
A Search for Novel Cancer/Testis Antigens in Lung Cancer Identifies VCX/Y Genes, Expanding the Repertoire of Potential Immunotherapeutic Targets
The Cancer Genome Atlas Dataset-Based Analysis of Aberrantly Expressed Genes by Geneanalytics in Thymoma Associated Myasthenia Gravis: Focusing on T Cells
Genetic Investigation in Non-Obstructive Azoospermia: from the X Chromosome to The
Top View
216141 2 En Bookbackmatter 461..490
January 2009 '!,$%2-!S2!."!89 Journal of the American Osteopathic College of Dermatology Journal of the American Osteopathic College of Dermatology
Relevance of Copy Number Variation at Chromosome X in Male Fetuses
Clinical and Molecular Characterization of Human Hereditary Disorders of Ectodermal Appendages
A Prenatal Diagnosis and Genetics Study of Five Pedigrees in the Chinese Population with Xp22.31 Microduplication
Expression and Localization of VCX/Y Proteins and Their Possible Involve- Ment in Regulation of Ribosome Assembly During Spermatogenesis
The Male-Specific Region of the Human Y Chromosome Is a Mosaic Of
Supplement to Cechova, Vegesna, Et Al
Supplementary Data 1
Banding Pattern on Polarized Hair Microscopic Examination and Unilateral Polymicrogyria in a Patient with Steroid Sulfatase Deficiency
Genome Science
Supplementary Table 1. a Full List of Cancer Genes
Histone H3.3K27M Mobilizes Multiple Cancer/Testis