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ANOS1
Blueprint Genetics ANOS1 Single Gene Test
Novel Mutations in ANOS1 and FGFR1 Genes Agnieszka Gach1* , Iwona Pinkier1, Maria Szarras-Czapnik2, Agata Sakowicz3 and Lucjusz Jakubowski1
Gene Expression Profiling of Corpus Luteum Reveals the Importance Of
Puberdade Precoce
Salsa MLPA Kit P002 BRCA1
CNTN5-/+ Or EHMT2-/+ Ipsc-Derived Neurons from Individuals With
Enabling Research with Human Embryonic and Fetal Tissue Resources Dianne Gerrelli1,*, Steven Lisgo2, Andrew J
Cellular-Resolution Gene Expression Profiling in the Neonatal Marmoset Brain Reveals Dynamic Species- and Region-Specific Differences
Study on Molecular Mechanism of ANOS1 Promoting Development of Colorectal Cancer
Defects in Gnrh Neuron Migration/Development and Hypothalamic-Pituitary Signaling Impact Clinical Variability of Kallmann Syndrome
Characterizing Genomic Duplication in Autism Spectrum Disorder by Edward James Higginbotham a Thesis Submitted in Conformity
Expanding the Genetic Spectrum of ANOS1 Mutations in Patients with Congenital Hypogonadotropic Hypogonadism
Dissecting the Genetics of Human Communication
ANOS1: a Unified Nomenclature for Kallmann Syndrome 1 Gene (KAL1) and Anosmin-1
Delayed Puberty
Importance of Growth Factor Diffusion in Sensory Organ Development 26 October 2018
Landscape of X Chromosome Inactivation Across Human Tissues Taru Tukiainen1,2, Alexandra-Chloé Villani2,3, Angela Yen2,4, Manuel A
Whole Genome Investigation of an Atypical Autism Case Identifies a Novel ANOS1 Mutation with Subsequent Diagnosis of Kallmann Syndrome
Top View
1 a Systematic Review and Standardized Clinical Validity Assessment of Male Infertility Genes 2 Running Title
A Case of Kallmann Syndrome Associated to a Novel Missense Mutation of the FGFR1 Gene
Gene Expression Profiling of Corpus Luteum Reveals Important
Extensive Cellular Heterogeneity of X Inactivation Revealed by Single-Cell Allele-Specific Expression in Human Fibroblasts. Marc
Fibroblast Growth Factor 2 Regulates Activity and Gene Expression of Human Post‐Mitotic Excitatory Neurons
Analysis of Genetic and Clinical Characteristics of a Chinese
Genomic and Transcriptomic Characterization of the Human Glioblastoma Cell Line AHOL1
Diagnosis and Treatment of Infertility in Men: AUA/ Tions Appear at the End of ASRM Guideline the Article
Key Genes Involved in Cell Cycle Arrest and DNA Damage Repair Identified in Anaplastic Thyroid Carcinoma Using Integrated Bioinformatics Analysis
ANOS1: a Unified Nomenclature for Kallmann Syndrome 1 Gene
New Genetic Findings in a Large Cohort of Congenital Hypogonadotropic Hypogonadism
From DNA Topology to Pubertal Onset: Using Integrative Genomic Approaches to Study Transcriptional Regulation
Genes Predisposing to Syndromic and Nonsyndromic Infertility: a Narrative Review Tajudeen O
2018 EAU Male Hypogonadism Search Strategy
Impact of Phosphodiesterase 4 Inhibition on the Operational Efficacy, Response Maxima and Kinetics of Indacaterol-Induced Gene Expression
Kallmann Syndrome
Fibroblast Growth Factor Receptors (Fgfrs) and Noncanonical Partners in Cancer Signaling
ANOS1: a Unified Nomenclature for Kallmann Syndrome 1 Gene (KAL1) and Anosmin-1
ANOS1 Gene Anosmin 1
European Consensus Statement on Congenital92n Hypogonadotropic Hypogonadism—Pathogenesis, Diag
The Epithelial-To-Mesenchymal Transition Regulates the E-Selectin Ligand Activities of Breast Cancer Cells a Dissertation Prese
YAP Regulates Cell Mechanics by Controlling Focal Adhesion Assembly