Master's in Genetic Counseling (MGC)
Independent Study Projects of MGC Program StudentsResearch for Beginners and a Case Example Development of a Booklet for Families of Individuals with Noonan Syndrome 
Survey of Master-Level Genetic Counseling Programs and Cancer Genetic Counselors Concerning Cancer Genetics and Cancer Genetic Counseling Training Physician Follow-Up of Normal Maternal Screening Results Survey of Parents of Children with Mucopolysaccharidoses and Mucolipidoses Concerning Medical Complications and Treatment Options Development of a Computer-Based Tutorial for Primary Care Physicians for The Management of Abnormal Newborn Screening Results Cancer Risk Perception, Management, and Role of Genetic Testing Among Men with a Family History of Breast Cancer The Impact of Genetic Testing in The Jewish Community Prader-Willi Syndrome Due to Maternal Uniparental Disomy and Suspected Trisomy 15 Mosaicism in a Liveborn Infant: A Case Report and Review Risk Factors of Coarctation of the Aorta with and without Ventricular Septal Defect: Analysis of the Baltimore-Washington Infant Study The Impact of a Genetic Diagnosis and Etiology of Mental Retardation or Learning Disabilities: A Survey of Special Educators An Evaluation of Different Recruitment Strategies Used in a Family Study Adolescent Referrals for Prenatal Genetic Counseling Services Depression and ApoE Genotypes in Young Adults with Down Syndrome Speech Patterns in Children with Kabuki Syndrome with and without Cleft Lip and/or Cleft Palate Does Hepatitis C Infection (HCV) Explain Otherwise Unexplained Elevated Maternal Serum Alpha-Fetoprotein (MSAFP) in Pregnant Women? The Role of the Physician in Family Decision Making: Enrollment of Adolescents in Genetic Susceptibility Research Genetic Differences in Tamoxifen Metabolizing Enzymes in Breast Cancer Patients Characterization of Psychiatric Patients Diagnosed with a 22q Deletion: Implications for Genetic Counseling The Relationship Between Genetic Counselors and Support Groups Supplemental Newborn Screening Using Tandem Mass Spectrometry: Attitudes of Parents, Pediatricians, and the Public of Maryland Down Syndrome and Autistic Spectrum Disorder: Prenatal, Neonatal and Neurological Risk Factors Surveying obstetric and neonatal nurses about carrier screening for cystic fibrosis Assessing the attitudes of physicians performing preimplantation genetic diagnosis toward controversial applications of this technology as a prenatal diagnostic tool The Predictive value of family history for Neuropsychiatric phenotypes in young adults with Down syndrome Incorporation of a Genetic Education Module and Its Impact on Students’ Genetic Knowledge and Role Definition: A Survey of Graduate Nursing Students Qualitative Study Investigating the Knowledge and Attitudes of Obstetricians Regarding Preimplantation Genetic Diagnosis Association Between Polymorphisms in Cytochrome P450CYP3A (CYP3A5) and Tamoxifen Metabolism in Breast Cancer Patients Group Study on Eighteen Children with Holoprosencephaly: Do Facial and Clinical Measurements Uphold or Refute the Face Predicting the Brain Assessment of the Effect of Prenatal Vitamin Use on AV Canal Defects in the Down Syndrome Population Behavioral Phenotype and Predictors of Maladaptive Behaviors in Cornelia de Lange Syndrome Comparison of the Dietitian and Genetic Counselor Professions As a Model for Professional Advancement I'd Rather Be FISHin': Detection of Chromosome 6q Abnormalities in Lymphoid Malignancies Using Fluorescence In Situ Hybridization Development of Educational Materials for First DegreeRelative of Individuals with UninformativeBRCA1/2 Test Results and Determining the Interest for Intervention and Support Health Providers’ Genetics Education: A Needs Assessment from Consumers of Genetics Services Primary Care Screening for Hereditary Cancers Assessing the Barriers to Newborn Screening in the Primary Care Setting Effects of Family History on the Quality of Life in Patients with Interstitial Cystitis A Parent’s Assessment of the Individual Educational Plan for Children with Down syndrome in Maryland Development of an Assay to Detect Pepsin in Respiratory Aspirates of Children to be used in the Diagnosis of Gastroesophageal Reflux Disease (GERD) Megan Skinner ‘06 Prevalence of Six Co-Morbid Non-Bladder Conditions in Multiplex Families with IC/PBS; a Case-Controlled Study Rebecca Crosetto ‘07 Comparing Family History Information as Recorded in a Family Medicine Chart Versus that Obtained by a Genetic Counselor Laura Krass ‘07 Core Competencies in Family History for All Health Care Professionals Emily Malouf ‘07 Current Resources, Methods, and Strategies for the Identification of Clinically Important Cytogenetic Abnormalities: A Survey and Independent Analysis Aimee Piurek ‘07 Prediction of Parenting Stress Levels Using Maladaptive Characteristics Observed in the Cornelia DeLange Syndrome Behavioral Phenotype Elizabeth Peterson Platt ‘07 An Examination of Sleep Disturbances in Cornelia DeLange Syndrome Georgette Saba ‘07 |
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