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Title:
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Condition:
--Any condition--
22q13.3 Deletion Syndrome
3M Syndrome
Aceruloplasminemia
Achondroplasia
Achromatopsia
Acrocephalosyndactyly
ADA Deficiency
Adrenoleukodystrophy
Advanced Maternal Age
Advanced Paternal Age
Agammaglobulinemia
Aicardi-Goutières Syndrome
Alagille Syndrome
Albinism
Alexander Disease
Alkaptonuria
Alpha Thalassemia
Alpha Thalassemia/Mental Retardation
Alpha-1 Antitrypsin Deficiency
Alport Syndrome
Alström Syndrome
Alzheimer Disease
Amyloid Polyneuropathy, Familial
Amyotrophic Lateral Sclerosis
Andersen-Tawil Syndrome
Androgen Insensitivity Syndrome
Anencephaly
Angelman Syndrome
Aniridia
Anxiety Disorders
Aortic Aneurysms, Thoracic
Arginase Deficiency
Argininosuccinase Synthetase Deficiency
Arginosuccinic Acid Lyase Deficiency
Asthma
Ataxia, Hereditary
Ataxia-Telangiectasia
Atelosteogenesis
Autism
Bardet-Biedl Syndrome
Basal Cell Nevus Syndrome
Basal Ganglia Calcification, Idiopathic, Familial
Beckwith-Wiedemann Syndrome
Beta Thalassemia
Biotinidase Deficiency
Birth Defects
Blepharophimosis Syndrome
Branchiootorenal Syndrome
BRCA1 & BRCA2
Brugada Syndrome
CACH
CADASIL
Camurati-Engelmann Disease
Canavan Disease
Cancer
Carbamyl Phosphate Synthetase Deficiency
Cardiovascular Disease
Carney Complex
Carnitine Palmitoyltransferase Deficiency
Cerebral Cavernous Malformations
Cerebral Palsy
Cerebrotendinous Xanthomatosis
Ceroid-Lipofuscinoses, Neuronal
Char Syndrome
Charcot-Marie-Tooth
Cholestasis, Progressive Familial Intrahepatic
Chondrodysplasia
Choreoacanthocytosis
Choroid Plexus Cyst
Choroideremia
Chromosome Abnormalities
Citrullinemia
Cleft Lip and Palate
Cleidocranial Dysplasia
Club Foot
Cockayne Syndrome
Coffin-Lowry Syndrome
Congenital Adrenal Hyperplasia
Congenital Adrenal Hypoplasia
Congenital Heart Defects
Congenital Hypothyroidism
Connexin 26
Contractural Arachnodactyly, Congenital
Craniosynostosis
Cystic Fibrosis
Cystinosis
Deafness
Dementia, Frontotemporal
Dementia, Presenile With Bone Cysts
Dentatorubral-Pallidoluysian Atrophy
Developmental Delay/Mental Retardation
Diabetes Insipidus, Nephrogenic
Down Syndrome
Dwarfism, Pituitary
Dysautonomia
Dystonia
Echogenic Bowel
Ectodermal Dysplasia
Ehlers-Danlos Syndrome
Encephalocele
Epidermolysis Bullosa
Epilepsy
Epiphyseal Dysplasia
Exostoses, Multiple
Fabry Disease
Familial Adenomatous Polyposis
Fanconi Anemia
Fetal Alcohol Syndrome
Fragile X Syndrome
Friedreich Ataxia
G6PD Deficiency
Galactosemia
Gastroschisis
Gaucher Disease
Genitalia/Urinary Tract Defects
Glucose Transport Defect, Blood-Brain Barrier
Glutaric Acidemia
Glycogen Storage Disease
Greig Cephalopolysyndactyly Syndrome
Hemochromatosis
Hemoglobin C
Hemoglobin E
Hemoglobin F (fetal)
Hemoglobin H Disease
Hemoglobin S
Hemoglobin Traits (not Sickle Cell)
Hemoglobinopathies
Hemophilia
Hemorrhagic Telangiectasia, Hereditary
Hereditary Nonpolyposis Colon Cancer
Heterotopia, Periventricular
Hirschsprung Disease
Holoprosencephaly
Homocystinuria
Huntington Disease
Hurler Syndrome
Hyperglycinemia
Hyperhomocysteinemia
Hyperinsulinism, Familial
Hyperkalemic Periodic Paralysis
Hyperlipoproteinemia
Hypochondroplasia
Hypokalemic Periodic Paralysis
Ichthyosis
Immunodeficiency
Incontinentia Pigmenti
Infertility
Isovaleric Acidemia
Jervell and Lange-Nielsen Syndrome
Joubert Syndrome
Ketone Utilization Disorder
Klinefelter Syndrome
Leber Optic Atrophy
Lesch-Nyhan Syndrome
Li-Fraumeni Syndrome
Lipodystrophy, Congenital
Long QT Syndrome
Lysosomal Disorders
Macular Dystrophy
Mannosidosis
Maple Syrup Urine Disease
Marfan Syndrome
Maternal PKU
MCAD
McKusick-Kaufman Syndrome
Mediterranean Fever, Familial
Megalencephalic Leukoencephalopathy
MELAS
Menkes Syndrome
MERRF
Metabolic Disorders
Microcephaly, Amish
Microphthalmia with Assoc. Anomalies
Migraine, Hemiplegic
Miscarriage/Stillbirth/Fetal Death
Mitochondrial Disorders
Mucopolysaccharidosis
Multicore Disease
Multiple Endocrine Neoplasia
Muscular Dystrophy
Myasthenia, Congenital
Myoclonic Dystonia
Myotonic Dystrophy
Myotubular Myopathy
Nail-Patella Syndrome
Nemaline Myopathy
Neural Tube Defects
Neurofibromatosis
Neuropathy, Giant Axonal
Neuropathy, Hereditary Sensory
Neurophathy, Liability to Pressure Palsies
Neutropenia, Congental, Cyclic
Niemann-Pick Disease
Nijmegen Breakage Syndrome
Noonan Syndrome
Norrie Disease
Occipital Horn Syndrome
Omphalocele
Ornithine Transcarbamylase Deficiency
Orofaciodigital Syndrome
Pallister-Hall Syndrome
Parkinson Disease
Pendred Syndrome
Peutz-Jeghers Syndrome
Phenylketonuria (PKU)
PKAN
Polycystic Kidney Disease
Polyposis, Juvenile Intestinal
Porphyria
Prader-Willi Syndrome
Prion Diseases
Prostate Cancer, Hereditary
Pseudoxanthoma Elasticum
PTEN Syndrome
Pulmonary Hypertension, Primary
Refsum Disease
Retinitis Pigmentosa
Retinoblastoma
Rett Syndrome
Rh Disease
Rothmund-Thomson Syndrome
Rubinstein-Taybi Syndrome
Russell-Silver Syndrome
Scheie Syndrome
Schizophrenia
Sclerosteosis
Severe Combined Immunodeficiency
Sickle Cell Anemia
Smith-Lemli-Opitz Syndrome
Smith-Magenis Syndrome
Spastic Paraplegia
Spastic Paraplegia, Hereditary
Spina Bifida
Spinal Muscular Atrophy
Spinocerebellar Ataxia
Spondylo-Epiphyseal Dysplasia
Stickler Syndrome
Tay-Sachs Disease
Thalassemia
Thrombophilia
Torsion Dystonia
Trisomy 13
Trisomy 18
Tuberous Sclerosis
Turner Syndrome
Tyrosinemia
Urea Cycle Disorder
Usher Syndrome
Velocardiofacial Syndrome
Von Hippel Lindau
Von Willebrand Disease
Waardenburg Syndrome
Werner Syndrome
Williams Syndrome
Wilson Disease
Wolf-Hirschhorn Syndrome
Xeroderma Pigmentosum
XXX
XYY
Subject:
Basic Genetics Information
Birth Defects Monitoring
Consumer Advocacy & Peer Support
Data
Consumer & Health Care Provider Genetics Education
Ethical Issues
Eugenics
Patenting
Privacy & Informed Consent
Research Policy
Other Ethical Issues
Evaluation of Services & Programs
Exposures During Pregnancy (Teratogens)
Financial & Economic Issues
Genetic Screening & Testing
Carrier Testing
DNA Banking
Newborn Screening
Prenatal Diagnosis
Presymptomatic & Predisposition Testing
Other Genetic Screening & Testing Issues
Genetics Services
Cultural Competency
Gene Therapy & Other Treatments
Indications for Referral
Services for Families with Genetic Conditions
Other Genetics Services Issues
Policy - Guidelines, Protocols, Position Statements, Consensus Statements
State Genetics Documents
Advisory Committees
State Genetics Plans
Other State Genetics Documents
Audience:
Consumers/Patients/Public
Professionals
Health Care Providers
Policy Makers/Public Health
Teachers
Other Professionals
Language:
To select multiple languages, hold down the Ctrl key (Apple key if you are on a Mac) while clicking on each one you want.
--Any language--
Arabic
Cambodian
Chinese
English
Farsi
French
French/Creole
Haitian Creole
Hmong
Khmer (Cambodian)
Korean
Laotian
Portuguese
Russian
Samoan
Spanish
Tagalog
Vietnamese
Format:
Brochures, pamphlets, booklets, fact sheets, comic/coloring books
Books, manuals, curricula, published articles, reports, policy statements/guidelines, forms
Videos, slides, posters
Organization:
--Any organization--
Agency for Healthcare Research and Quality
Air Force Medical Genetics Center
Alaska Health and Social Services
American Academy of Family Physicians
American Academy of Pediatrics
American Association for the Study of Liver Diseases
American Cancer Society
American College of Medical Genetics
American College of Obstetricians and Gynecologists
American Gastroenterological Association
American Medical Association
American Pain Society
American Society of Clinical Oncology
American Society of Colon and Rectal Surgeons
American Society of Gene Therapy
American Society of Human Genetics
American Society of Law, Medicine & Ethics
American Society of Reproductive Medicine
American Thoracic Society
Arizona Department of Health Services
Assoc. of Asian/Pacific Community Health Organizations
Assoc. of Genetic Technologists
Assoc. of Maternal and Child Health Programs
Assoc. of Professors of Human or Medical Genetics
Assoc. of Public Health Laboratories
Assoc. of Schools of Public Health
Assoc. of State and Territorial Health Officials
Assoc. of Women's Health, Neonatal and Obstetric Nurses
California Department of Health Services
CDC - Centers for Disease Control and Prevention
CDC - Division of AIDS, STD, and TB Laboratory Research
CDC - Division of Laboratory Systems
CDC - Division of Nutrition & Physical Activity
CDC - Human Genome Epidemiology Network
CDC - Morbidity and Mortality Weekly Report
CDC - National Center for Birth Defects and Developmental Di
CDC - Office of Genomics & Disease Prevention
CDC-National Birth Defects Prevention Network
Charles C. Thomas - Publisher, Ltd.
Children's Hospital Medical Center of Akron
Children's Hospital of Wisconsin
Children's Medical Center, The
Colorado Department of Public Health and Environment
Computer Sciences Corporation
Cooley's Anemia Foundation, Inc.
Council of Regional Networks for Genetic Services
Council of State and Territorial Epidemiologists
Council of State Governments
Dartmouth Medical School
Department of Health and Human Services
Elwyn, Inc.
Emory University
Endocrine Society, The
Florida Department of Health & Rehabilitative Services
Foundation for Blood Research
GeneReviews/GeneTests
Genetic Alliance
Genetic Education Materials Database
Georgetown University
Georgia Division of Public Health
Great Lakes Regional Genetics Group - GLaRGG
Great Plains Genetics Service Network - GPGSN
Hawaii Department of Health
Health Resources and Services Administration Information Cen
Health Systems Research
Illinois Department of Public Health
Indiana State Department of Health
Institute for Child Health Policy
International Collaborative Gaucher Group
Iowa Department of Public Health
Joint Center for Sickle Cell and Thalassemic Disorders
Kaiser Permanente
Kendall/Hunt Publishing Company
Lippincott Williams & Wilkins
LTG Associates, Inc.
March of Dimes Birth Defects Foundation
Maryland Department of Health & Mental Hygiene
Massachusetts Department of Public Health
MCHB - Division of Services for Children with Special Needs
MCHB - Genetics Services Branch
MCHB - Maternal and Child Health Bureau
Medical College of Virginia
Michigan Department of Community Health
Mid-Atlantic Regional Human Genetics Network - MARHGN
Milbank Memorial Fund
Minnesota Department of Health
Mississippi State Department Of Health
Missouri Department of Health and Senior Services
Mountain States Genetics Network - MoSt GeNe
National Association of Social Workers
National Coalition for Health Professional Education in Gene
National Conference of State Legislatures
National Council on Disability
National Hemophilia Foundation
National Newborn Screening and Genetics Resource Center
National Organization for Rare Disorders
National Society of Genetic Counselors
Nebraska Department of Health and Human Services
New England Newborn Screening Program
New England Regional Genetics Group - NERGG
New Jersey Hospital Association
New York State Department of Health
NIH - Consensus Program Information Center
NIH - National Cancer Institute
NIH - National Heart, Lung and Blood Institute
NIH - National Human Genome Research Institute
NIH - National Institute of Child Health and Human Developme
NIH - National Institute of Diabetes & Digestive & Kidney Di
NIH - National Library of Medicine - NICHSR
NIH - Office of Biotechnology Activities
North Carolina Department of Health and Human Services
Northern California Comprehensive Thalassemia Center
Oak Ridge National Laboratory
Office of Technology Assessment
Ohio Department of Health
Oklahoma State Department of Health
Oregon Department of Human Services
Organization of Teratology Information Services
Oxford University Press
Pacific Northwest Regional Genetics Group - PacNoRGG
Pacific Southwest Regional Genetics Network - PSRGN
Preimplantation Genetics Diagnosis International Society
Primary OB Genetic Risk Assessment and Management in Maine
Public Health Foundation
Public Health Reports/Oxford University Press
Rand Reed Group, The
Reproductive Biomedicine Online
Rhode Island Department of Health
S. Karger's Medical and Scientific Publishers
Schleicher and Schuell BioScience, Inc.
Screening, Technology, and Research in Genetics
Secretary's Advisory Committee on Genetic Testing
Shriver Center
Sickle Cell Disease Association of America, Inc.
Sickle Cell Information Center, The
Society of Teachers of Family Medicine
Southeastern Regional Genetics Group
Tennessee Department of Health
Texas Department of State Health Services
Texas Genetics Network - TEXGENE
Texas Medical Association
United States General Accounting Office
United States Government Printing Office
University of Arizona
University of Kentucky
University of Medicine and Dentistry of New Jersey
University of Michigan School of Public Health
University of South Dakota
University of Washington - Center for Genomics and Public He
University of Washington Medical Center
University of Wisconsin Medical School
Utah Department of Health
Vanderbilt University Medical Center
W.B. Saunders
Washington State Department of Health
White House, The
Wiley-Liss, Inc.
OR