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MAB21L2
BMC Cell Biology Biomed Central
MAB21L1 Loss of Function Causes a Syndromic Neurodevelopmental Disorder with Distinctive Cerebellar, Ocular, Craniofacial and Ge
Foraging Shifts and Visual Pre Adaptation in Ecologically Diverse Bats
A Radiation Hybrid Map of Chicken Chromosome 4
Transcriptome Analysis of Nautilus and Pygmy Squid Developing Eye Provides Insights in Lens and Eye Evolution
DNA Methylation Perturbations May Link Altered Development and Aging in the Lung
Milger Et Al. Pulmonary CCR2+CD4+ T Cells Are Immune Regulatory And
Produktinformation
The Bioplex Network: a Systematic Exploration of the Human Interactome
Mb 4Q22.2Q32.3 Duplication Due to Ovarian Germinal Mosaicism
An Evolutionarily Conserved Nested Gene Pair — Mab21 and Lrba/Nbea in Metazoan
Molecular Genetic Delineation of a Deletion of Chromosome 13Q12→Q13 in a Patient with Autism and Auditory Processing Deficits
Genetic Landscape of Joubert Syndrome in French Canadians
Autosomal Recessive Coding Variants Explain Only a Small Proportion of Undiagnosed Developmental Disorders in the British Isles
The Transcriptional Profile of Mesenchymal Stem Cell Populations in Primary Osteoporosis Is Distinct and Shows Overexpression of Osteogenic Inhibitors
Unveiling Genomic Regions That Underlie Differences Between Afec
Zebrafish Models of Rare Hereditary Pediatric Diseases
Differential Expression of Meis2, Mab21l2 and Tbx3 During Limb Development Associated with Diversification of Limb Morphology in Mammals
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Identification of Core Genes and Prediction of Mirnas Associated with Osteoporosis Using a Bioinformatics Approach
Supplementary Table 1. a Full List of Cancer Genes