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- A Targeted Next-Generation Sequencing Assay for the Molecular
- DAPA 741 Oral Pathology Examination 4 December 6, 2000 1
- Download CGT Exome V2.0
- Rare Disease Conditions Eligibility Criteria 100,000 Genomes Project Document Key: PAR-GUI-058 Version: 1.9.0
- Single Gene Disorders with Craniofacial and Oral Manifestations 1Shankargouda Patil, 2Roopa S Rao, 3Barnali Majumdar
- Genomeposter2009.Pdf
- 1 – Ust-Dzhegutinsky District; 2
- SYSTEMIC DISORDERS AFFECTING DENTAL PATHOLOGY 249 Be Associated to Dental Discoloration
- Genomic Studies in the Field of Dentistry – an Indian Scenario Raghu Dhanapal* Department of Oral & Maxillofacial Pathology, I.T.S Dental College and Hospital, India
- (Orofaciodigital Syndrome (Type I) (X-Linked
- Blindness, Hearing Loss and Brown Crumbly Teeth: Determining the Molecular Basis of Heimler and Heimler Plus Syndromes and Other Related Conditions
- Amelogenesis Imperfecta May Also Be Clinically Associated with Rare Observation
- Incontinentia Pigmenti: a Case Report R
- SNODENT (Systemized Nomenclature of Dentistry)
- Surgeon General's Report on Oral Health in America
- Oral Dermatology from a to Z
- Amelogenesis Imperfecta [PDF]
- Health Issues Index
- Dental Development in Amelogenesis Imperfecta
- Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
- Amelogenesis Imperfecta; Genes, Proteins, and Pathways
- Nonodontogenic Sources of Dental Pain
- ORPHA Number Disease Or Group of Diseases 300305 11P15.4
- JCNDE.Org: INBDE Item Development Guide Appendices
- Basic Principles of Human Genetics: a Primer for Oral Medicine Harold C
- Panoramic Radiographic Evaluation of Dental Anomalies, Dental Mineralization Stage, and Mandibular Angle
- Carriers with Functional Null Mutations in LAMA3 Have Localized Enamel Abnormalities Due to Haploinsufficiency
- Monogenic Disorders
- Amelogenesis Imperfecta, Hypoplastic Type Associated with Some Dental Abnormalities: a Case Report
- Sex Chromosomes in Human Tooth Root Growth. Radiographic Studies On
- Klinefelter Syndrome in Childhood: Variability in Clinical and Molecular Findings
- A 27-Year-Old Man with Severe Osteoporosis and Multiple Bone Fractures
- Asymmetrical Tooth Defects Observed in Hypoplastic Primary Teeth and Amelogenesis Imperfecta: Case Reports
- Rare Disease Registries in Europe
- Amelogenesis Imperfecta - in BRIEF • Outlines the Clinical Presentation of Amelogenesis Imperfecta (AI) and How to PRACTICE Lifelong Management
- Identification of a Homozygous PEX26 Mutation in a Heimler Syndrome
- 14 AP Genetics
- Zellweger Spectrum Disorders
- Oral Pathology: a Clinical Review
- EPITHELIAL PATHOLOGY from a to Z and Systemic Considerations: What Every Clinician Should Know
- Genes Involved in Amelogenesis Imperfecta. Part I
- Guideline on Oral Health Care/Dental Management of Heritable Dental Developmental Anomalies
- Application of the International Classification of Diseases to Dentistry and Stomatology
- Blueprint Genetics Amelogenesis Imperfecta and Dentinogenesis
- 4. Oral Pathology
- Download Gene List
- Sex-Linked Genetic Diseases52
- Herpesvirus Infections
- Amelogenesis Imperfecta
- OMIM Mendelian Gene List V2.0
- Management of Amelogenesis Imperfecta in Childhood: Two Case Reports
- Recessive Gene List V2.0
- Genetic Diagnostics Test(S)/Gene(S)/Panel(S)
- Disease ID Disorder Name Gene Symbols OMIM ID