| Screening Behavior in Adults With Hereditary Hemorrhagic Telangiectasia (NCT00684879) | National Human Genome Research Institute (NHGRI) | 2008-05-21 |
| Adaptation and Quality of Life Among Adults With Neurofibromatosis Type I (NCT00684398) | National Human Genome Research Institute (NHGRI) | 2008-05-15 |
| The Experience of Caregivers of Children With Down Syndrome (NCT00695695) | National Human Genome Research Institute (NHGRI) | 2008-05-14 |
| Patient Provider Communication and Interaction in a Virtual Clinical Setting (NCT00669188) | National Human Genome Research Institute (NHGRI) | 2008-04-24 |
| Studies of Skin Microbes in Healthy People and in People With Skin Conditions (NCT00605878) | National Human Genome Research Institute (NHGRI) | 2008-01-22 |
| Making Sense of a Positive Genetic Test Result for Huntington Disease (NCT00539747) | National Human Genome Research Institute (NHGRI) | 2007-10-01 |
| Informed Choice Regarding Invasive Prenatal Testing (NCT00514553) | National Human Genome Research Institute (NHGRI) | 2007-08-07 |
| Treatment Strategies for Children With Smith-Magenis Syndrome (NCT00506259) | National Human Genome Research Institute (NHGRI) | 2007-07-17 |
| Predictors of Caregiver Adaptation to Pervasive Developmental Disorders (NCT00496210) | National Human Genome Research Institute (NHGRI) | 2007-06-27 |
| Individuals Patterns of Disclosure About Huntington s Disease (HD) and the Association With Adaptation to HD (NCT00491842) | National Human Genome Research Institute (NHGRI) | 2007-06-22 |
| African American Families and Lung Cancer Study (NCT00487760) | National Human Genome Research Institute (NHGRI) | 2007-06-11 |
| Disclosing a Cystic Fibrosis Diagnosis to a Dating Partner (NCT00485082) | National Human Genome Research Institute (NHGRI) | 2007-06-05 |
| Risk Communication Within Mexican-American Families (NCT00469339) | National Human Genome Research Institute (NHGRI) | 2007-04-27 |
| Pilot Study of a Multi-Drug Regimen for Severe Pulmonary Fibrosis in Hermansky-Pudlak Syndrome (NCT00467831) | National Human Genome Research Institute (NHGRI) | 2007-04-01 |
| Interventions to Educate An Underserved Population About Inherited Disease Risks (NCT00441077) | National Human Genome Research Institute (NHGRI) | 2007-02-19 |
| ClinSeq: A Large-Scale Medical Sequencing Clinical Research Pilot Study (NCT00410241) | National Human Genome Research Institute (NHGRI) | 2007-01-05 |
| Genetic Counselors' Experiences of Moral Value Conflicts With Clients (NCT00360711) | National Human Genome Research Institute (NHGRI) | 2006-06-01 |
| Positron Emission Tomography (PET) Imaging in People With Gaucher Mutations (NCT00302146) | National Human Genome Research Institute (NHGRI) | 2006-05-23 |
| Patients' Perspectives on Identity, Ancestry and Genetics (NCT00359710) | National Human Genome Research Institute (NHGRI) | 2006-04-19 |
| Use of Virtual Reality to Communicate Concepts of Genomics to the General Public (NCT00316056) | National Human Genome Research Institute (NHGRI) | 2006-04-14 |
| Invasive Prenatal Testing Decisions in Pregnancy After Infertility (NCT00341822) | National Human Genome Research Institute (NHGRI) | 2006-03-29 |
| Experiences of Genetics Patients With Visible Abnormalities Who Facilitate Teaching in Genetics Clinics (NCT00341718) | National Human Genome Research Institute (NHGRI) | 2006-03-29 |
| Perspectives of Individuals With Bipolar Disorder and Siblings of Individuals With Bipolar Disorder; A Telephone Interview Study (NCT00300820) | National Human Genome Research Institute (NHGRI) | 2006-03-02 |
| Psychosocial Aspects of Genetic Testing for Hereditary Nonpolyposis Colon Cancer (NCT00341575) | National Human Genome Research Institute (NHGRI) | 2005-09-28 |
| Intravenous Immune Globulin to Treat Hereditary Inclusion Body Myopathy (NCT00195637) | National Human Genome Research Institute (NHGRI) | 2005-09-16 |
| Physicians' Understanding of Human Genetic Variation (NCT00339924) | National Human Genome Research Institute (NHGRI) | 2005-07-11 |
| Positive Exposure: A Photography and Video Intervention for Individuals With Craniofacial Differences (NCT00340964) | National Human Genome Research Institute (NHGRI) | 2005-06-13 |
| Developing Newborn Screening for Infants With Primary Immunodeficiency (NCT00113464) | National Human Genome Research Institute (NHGRI) | 2005-06-02 |
| Clinical Study of Muenke Syndrome (FGFR3-Related Craniosynostosis) (NCT00106977) | National Human Genome Research Institute (NHGRI) | 2005-03-31 |
| Analysis of Data From the Women's Contraceptive and Reproductive Experiences (CARE) Study (NCT00341159) | National Human Genome Research Institute (NHGRI) | 2005-01-18 |
| Genetic Analysis of Craniosynostosis, Philadelphia Type (NCT00367796) | National Human Genome Research Institute (NHGRI) | 2005-01-05 |
| Genetic Analysis of Craniofrontonasal Syndrome (NCT00339846) | National Human Genome Research Institute (NHGRI) | 2005-01-05 |
| Long-Term Study of Nitisinone to Treat Alkaptonuria (NCT00107783) | National Human Genome Research Institute (NHGRI) | 2005-01-01 |
| Prevalence of Ambivalence Regarding Prenatal Testing (NCT00342069) | National Human Genome Research Institute (NHGRI) | 2004-12-17 |
| Impact of Lung Cancer Diagnosis on Relatives' Understanding of Genetic Risk and Receptivity to Quit Smoking (NCT00341341) | National Human Genome Research Institute (NHGRI) | 2004-12-07 |
| Clinical Integration of Genetic Risk Assessment in Family Medicine (NCT00339794) | National Human Genome Research Institute (NHGRI) | 2004-12-07 |
| Identification of Prostate Cancer Genes (NCT00342784) | National Human Genome Research Institute (NHGRI) | 2004-11-08 |
| Clinical Studies of Progeria (NCT00094393) | National Human Genome Research Institute (NHGRI) | 2004-10-14 |
| Study of Megakaryocytes From Patients With Abnormal Platelet Vesicles (NCT00086476) | National Human Genome Research Institute (NHGRI) | 2004-06-29 |
| Analysis of Specimens From Individuals With Pulmonary Fibrosis (NCT00084305) | National Human Genome Research Institute (NHGRI) | 2004-06-09 |
| Clinical and Laboratory Study of Methylmalonic Acidemia (NCT00078078) | National Human Genome Research Institute (NHGRI) | 2004-06-07 |
| Genetics and Clinical Characteristics of Bardet-Biedl Syndrome (NCT00078091) | National Human Genome Research Institute (NHGRI) | 2004-02-17 |
| Genetic Studies in the Amish and Mennonites (NCT00359580) | National Human Genome Research Institute (NHGRI) | 2004-02-10 |
| Clinical and Genetic Studies on Holoprosencephaly (NCT00088426) | National Human Genome Research Institute (NHGRI) | 2004-01-23 |
| Cell Studies of Parkinson's Disease (NCT00076505) | National Human Genome Research Institute (NHGRI) | 2004-01-14 |
| Influence of Genetics on Vitamin Metabolism in Pregnant Women (NCT00340366) | National Human Genome Research Institute (NHGRI) | 2003-12-16 |
| Genetic Studies of Inflammatory Bowel Disease (NCT00340444) | National Human Genome Research Institute (NHGRI) | 2003-11-06 |
| Immunogenetics of Visceral Leishmaniasis (NCT00342823) | National Human Genome Research Institute (NHGRI) | 2003-10-20 |
| Genetic Analysis of Gray Platelet Syndrome (NCT00069680) | National Human Genome Research Institute (NHGRI) | 2003-09-29 |
| Genetic Epidemiology of Lung Cancer (NCT00341835) | National Human Genome Research Institute (NHGRI) | 2003-08-26 |
| The Value of Genetic Information to Adult Adopted Individuals (NCT00057694) | National Human Genome Research Institute (NHGRI) | 2003-04-01 |
| Clinical and Molecular Investigations Into Ciliopathies (NCT00068224) | National Human Genome Research Institute (NHGRI) | 2003-03-16 |
| Transitional Life Events in Patients With Friedreich's Ataxia: Implications for Genetic Counseling (NCT00056186) | National Human Genome Research Institute (NHGRI) | 2003-03-01 |
| Family Studies of Eye Traits (NCT00342342) | National Human Genome Research Institute (NHGRI) | 2002-12-04 |
| Pilot Study of the Process of Prenatal Genetic Counseling (NCT00047905) | National Human Genome Research Institute (NHGRI) | 2002-10-01 |
| Study of Chediak-Higashi Syndrome (NCT00005917) | National Human Genome Research Institute (NHGRI) | 2002-09-10 |
| Family Myopia Study (NCT00341549) | National Human Genome Research Institute (NHGRI) | 2002-04-29 |
| Genetic Analysis of Fraser Syndrome and Fryns Syndrome (NCT00032877) | National Human Genome Research Institute (NHGRI) | 2002-04-01 |
| Exploratory Data Analysis for Disease Pedigrees and Cancer Genetics (NCT00339508) | National Human Genome Research Institute (NHGRI) | 2002-03-19 |
| Natural History of Glycosphingolipid Storage Disorders and Glycoprotein Disorders (NCT00029965) | National Human Genome Research Institute (NHGRI) | 2002-02-06 |
| Analysis of Prostate Cancer Short-Term Cultures Using Molecular Cytogenetic Methods (NCT00022919) | National Human Genome Research Institute (NHGRI) | 2001-08-01 |
| Gene Transfer Therapy for Severe Combined Immunodeficieny Disease (SCID) Due to Adenosine Deaminase (ADA) Deficiency (NCT00018018) | National Human Genome Research Institute (NHGRI) | 2001-06-20 |
| Natural History Study of Smith-Magenis Syndrome (NCT00013559) | National Human Genome Research Institute (NHGRI) | 2001-03-19 |
| Molecular Analysis of Microphthalmia/Anophthalmia (NCT00011843) | National Human Genome Research Institute (NHGRI) | 2001-02-22 |
| Genetic Analysis of Oculocerebrorenal Syndrome of Lowe (NCT00359515) | National Human Genome Research Institute (NHGRI) | 2001-02-17 |
| Genetic Analysis of Familial Brain Aneurysms (NCT00011856) | National Human Genome Research Institute (NHGRI) | 2001-02-01 |
| Molecular and Clinical Studies of Primary Immunodeficiency Diseases (NCT00006319) | National Human Genome Research Institute (NHGRI) | 2000-10-25 |
| Influences on Female Adolescents' Decisions Regarding Testing for Carrier Status of XSCID (NCT00006335) | National Human Genome Research Institute (NHGRI) | 2000-09-26 |
| Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion Bodies (NCT00006176) | National Human Genome Research Institute (NHGRI) | 2000-08-10 |
| Risk Evaluation and Education for Alzheimer's Disease (NCT00571025) | National Human Genome Research Institute (NHGRI) | 2000-08-01 |
| Study of Alkaptonuria (NCT00005909) | National Human Genome Research Institute (NHGRI) | 2000-06-21 |
| Study of the Experiences and Needs of Parents Continuing a Pregnancy Following a Prenatal Diagnosis of Holopresencephaly (NCT00005016) | National Human Genome Research Institute (NHGRI) | 2000-03-01 |
| Gene Therapy and Ganciclovir in Treating Patients With Stage IV Melanoma (NCT00005057) | National Human Genome Research Institute (NHGRI) | 2000-03-01 |
| Genetic Analysis of Attention Deficit Hyperactivity Disorder (ADHD) (NCT00046059) | National Human Genome Research Institute (NHGRI) | 2000-02-08 |
| Study of the Results of Education and Counseling for Persons Undergoing Genetic Testing for Hereditary Nonpolyposis Colon Cancer (NCT00004210) | National Human Genome Research Institute (NHGRI) | 2000-02-01 |
| Genetic Analysis of Neural Tube and Orofacial Cleft Defects in the Irish Population (NCT00341068) | National Human Genome Research Institute (NHGRI) | 2000-01-01 |
| Mind-Body Therapy for Pain in Ehlers-Danlos Syndrome (NCT00001966) | National Human Genome Research Institute (NHGRI) | 2000-01-01 |
| Genetic Analysis of Left-Right Axis Formations (NCT00341133) | National Human Genome Research Institute (NHGRI) | 1999-12-13 |
| Microarray Analysis for Human Genetic Disease (NCT00001898) | National Human Genome Research Institute (NHGRI) | 1999-06-29 |
| Lung Disease Associated With Rheumatoid Arthritis (NCT00001876) | National Human Genome Research Institute (NHGRI) | 1999-04-05 |
| Genetic Analysis of Familial Melanoma (NCT00339404) | National Human Genome Research Institute (NHGRI) | 1999-03-04 |
| Study of Skeletal Disorders and Short Stature (NCT00001754) | National Human Genome Research Institute (NHGRI) | 1998-06-01 |
| Genetic Analysis of Hereditary Non-Syndromic Oral Clefts (NCT00340626) | National Human Genome Research Institute (NHGRI) | 1997-08-31 |
| Gene Analysis of Parkinson's Disease (NCT00001643) | National Human Genome Research Institute (NHGRI) | 1997-08-29 |
| Positional Cloning of the Gene(s) Responsible for Alagille Syndrome (NCT00001642) | National Human Genome Research Institute (NHGRI) | 1997-05-01 |
| Study of Heritable Connective Tissue Disorders (NCT00001641) | National Human Genome Research Institute (NHGRI) | 1997-03-01 |
| Genetic Analysis of Parkinson's Disease (NCT00001640) | National Human Genome Research Institute (NHGRI) | 1997-02-11 |
| Evaluation of Patients With Unresolved Chromosome Abnormalities (NCT00001639) | National Human Genome Research Institute (NHGRI) | 1996-12-01 |
| Issues Surrounding Prenatal Genetic Testing for Achondroplasia (NCT00001536) | National Human Genome Research Institute (NHGRI) | 1996-08-01 |
| Mapping Genes for Type 2 (Non-Insulin Dependent) Diabetes Mellitus (NCT00339885) | National Human Genome Research Institute (NHGRI) | 1996-06-01 |
| Twins Study of Gene Therapy for HIV Infection (NCT00001535) | National Human Genome Research Institute (NHGRI) | 1996-03-01 |
| Clinical and Basic Investigations Into Hermansky-Pudlak Syndrome (NCT00001456) | National Human Genome Research Institute (NHGRI) | 1995-11-06 |
| Genetic Studies of Lysosomal Storage Disorders (NCT00001215) | National Human Genome Research Institute (NHGRI) | 1995-03-08 |
| Outcomes of Education and Counseling for BRCA1 Testing (NCT00001468) | National Human Genome Research Institute (NHGRI) | 1995-03-01 |
| Genetic Analysis of Hereditary Prostate Cancer (NCT00001469) | National Human Genome Research Institute (NHGRI) | 1995-01-01 |
| Study of Clinical and Molecular Manifestations of Genetic Disorders (NCT00001466) | National Human Genome Research Institute (NHGRI) | 1994-10-01 |
| Phenotype and Etiology of Pallister-Hall Syndrome (NCT00001404) | National Human Genome Research Institute (NHGRI) | 1994-08-18 |
| Study of Proteus Syndrome and Related Congenital Disorders (NCT00001403) | National Human Genome Research Institute (NHGRI) | 1994-04-27 |
| Familial Mediterranean Fever and Related Disorders: Genetics and Disease Characteristics (NCT00001373) | National Human Genome Research Institute (NHGRI) | 1994-03-10 |
| Gene Transfer Therapy for Severe Combined Immunodeficieny Disease (SCID) Due to Adenosine Deaminase (ADA) Deficiency: A Natural History Study (NCT00001255) | National Human Genome Research Institute (NHGRI) | 1990-09-01 |