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- Medical Genetics and Genomics Milestones
- Factor II/Prothrombin Testing for Thrombophilia
- American College of Medical Genetics Consensus Statement on Factor V Leiden Mutation Testing
- Whole Exome and Whole Genome Sequencing
- Variants and Health
- BRCA Mutation Screening and Patterns Among High-Risk Lebanese
- A Statement of the American College of Medical Genetics and Genomics (ACMG)
- Molecular Genetic Pathology (Effective: July 1, 2017) Review Committees for Medical Genetics and Genomics and Pathology ACGME
- Phelan-Mcdermid Syndrome (22Q13 Deletions)
- Glossary of Genetic Terms Used in This Review
- Genetics: Size of 22Q13 Deletion Predicts Clinical Features
- Basic Concepts in Medical Genetics: Mendelian and Non-Mendelian Genetics and the Rise of the New Technologies
- Bioinformatics Methods in Medical Genetics and Genomics
- Editorial Highlights on Medical Genetics of Infection (Special Issue)
- BRCA Analysis
- Master's Program in Medical Sciences
- Medical Genetics and Genomics, Ms
- BRCA1 and BRCA2 Genetic Testing – Medicare Advantage Policy
- Consensus Guideline on Genetic Testing for Hereditary Breast Cancer
- A Systematic Literature Review of Behavioral Interventions for Phelan-Mcdermid Syndrome Kate Anne Schroeder St
- Whole Exome and Whole Genome Sequencing
- Translating Advances in Human Genetics Into Public Health
- Medical Necessity Guidelines: Genetic Testing: BRCA-Related Breast And/Or Ovarian Cancer Syndrome Effective: October 21, 2020
- Medical Bacteriology and Medical Genetics, 1880–1940: a Call for Synthesis
- Strategic Plan for the Roundtable on Genomics and Precision Health
- Identification of Novel L2HGDH Gene Mutations and Update Of
- Factor V Leiden, Prothrombin G20210A Substitution and Hormone
- The Intersection of Genetics and COVID-19 in 2021: Preview of the 2021 Rodney Howell Symposium Sonja A
- Review of Ethical Issues in Medical Genetics
- Delineation of the Genetic and Clinical Spectrum of Phelan-Mcdermid Syndrome Caused by SHANK3 Point Mutations Silvia De Rubeis1,2† , Paige M
- Medical Genetics This Document Was Endorsed by the American Academy of Family Physicians (AAFP)
- Genetic Testing for Hereditary Breast And/Or Ovarian Cancer Screening (HBOC)
- Lesson 3: Genetics
- Can Factor V Leiden
- Co-Morbidity of Sanfilippo Syndrome Type C and D-2-Hydroxyglutaric
- Whole Genome Sequencing
- Molecular and Medical Genetics
- Whole Exome and Whole Genome Sequencing
- Whole Exome and Whole Genome Sequencing
- Draft Genetic Test Review[PDF 987KB]
- The Case for Personalized Medicine
- Molecular and Medical Genetics Grand Rounds 2012 - 2013 Grand Rounds Schedule Thursdays, 9:00 to 10:00 A.M., Mac Hall 3198
- Corporate Medical Policy
- Medical Genetics and Genomics
- PE2386 Medical Genetics
- Priorities of Clinical Genetics in Translational Biomedicine Wilson Mendy*
- Outline of a Medical Genetics Curriculum for Internal Medicine Residency Training Programs Douglas L
- Genetics and Molecular Pathology Laboratory Services User Information Manual
- The Rise of the Genome and Personalised Medicine
- Genetic Pathology Medical Genomics Trainee Handbook 2021
- Medical Genetics Profile
- Medical Genetics
- Identification of Novel L2HGDH Mutation in a Large Consanguineous
- Master of Medical Genetics
- Understanding Genetics
- The Potential and Limits of Personalized Medicine Position Paper Issued by the Swiss Academy of Medical Sciences1
- The Genetics of Thrombophilia Written By: Elizabeth Varga, M.S.*
- Regional Genetics Resource Directory
- 1 I. Introduction Welcome to the Medical Genetics and Genomics
- Molecular Genetic Pathology Fellowship
- 22Q13.2Q13.32 Genomic Regions Associated with Severity of Speech Delay, Developmental Delay, and Physical Features in Phelan–Mcdermid Syndrome
- Factor II/Prothrombin Testing for Thrombophilia
- Lessons Learned from the Introduction of Personalized Genotyping Into a Medical School Curriculum David R