Master's in Genetic Counseling (MGC)
Independent Study Projects of MGC Program Students
Research 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)
Comparing Family History Information as Recorded in a Family Medicine Chart Versus that Obtained by a Genetic Counselor
Core Competencies in Family History for All Health Care Professionals
Current Resources, Methods, and Strategies for the Identification of Clinically Important Cytogenetic Abnormalities: A Survey and Independent Analysis
Prediction of Parenting Stress Levels Using Maladaptive Characteristics Observed in the Cornelia DeLange Syndrome Behavioral Phenotype
An Examination of Sleep Disturbances in Cornelia DeLange Syndrome
Prevalence of Six Co-Morbid Non-Bladder Conditions in Multiplex Families with IC/PBS; a Case-Controlled Study
Determination of Risk Assessment Protocols or Midtrimester Amniocentesis in Prenatal Care Centers
The Use of Invasive Prenatal Diagnostic Tests in Patients with a History of Infertility
The Mother-Daughter Breast Cancer Connection: Risk Perception, Cancer Worry and Impact of Event Study
Assessment of Physicians’ Screening Practices and Knowledge of Genetic Disorders in the Ashkenazi Jewish Population
Attitudes of Genetic Counselors Toward a Pictorial Representation of Genetic Disease |
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