Andrew's Buddies - Fight Spinal Muscular Atrophy
Andrew's Buddies fights spinal muscular atrophy, the leading genetic and inherited cause of infant death. We fund neuromuscular research and SMN, SMA non-profit drug trials....

Angelman Syndrome Foundation (ASF)
Foundation established to help answer questions and provide a network of information, education and support resources to Angelman Syndrome families and friends....

Ataxia-Telangiectasia (A-T) Society
Welcome to the website of the Ataxia-Telangiectasia Society ("A-T Society")....

Carolina Fragile X Project
studies examining the impact of fragile X syndrome (FXS) on individuals, families & the agencies that serve them. FPG Child Development Institute• University of North Carolina at Chapel Hill...

CdLS-USA Outreach
The Cornelia de Lange Syndrome (CdLS) Foundation is a nonprofit [501 (c) (3)] voluntary health organization based in Avon, Connecticut (USA)....

Celera
The online information business is a leading provider of information based on the human genome and related biological and medical information....

CHARGE Syndrome Foundation
"CHARGE" came from the first letter: C = coloboma, H = heart defects, A = atresia of the choanae, R = retardation of growth development, G = genital and urinary abnormalities, E = ear abnormality ...

Chromosome 22 Central
A support group for families who have children affected by disorders involving chromosome 22....

Chromosome Deletion Outreach, Inc. (CDO) Rare Chromosome Disorder Support
Chromosome Deletion Outreach, Inc. (CDO) is a non-profit organization for families affected by any type of rare chromosome disorder: deletions, translocations, trisomies, rings and inversions...

Cri du Chat Support Group of Australia Inc.
The Cri Du Chat Support Group of Australia Inc....

Cri du Chat Syndrome Support Group
The Cri du Chat Syndrome Support Group...

Cystic Fibrosis Trust Website
Funding research to understand, treat and cure Cystic Fibrosis. The UK's most common life-threatening inherited disease...

DNA jobs
Post & Search Biotechnology, Medical, and Life Sciences Jobs and Resumes for Free at DNAjobs.com...

DNA Sciences
Genetic Discovery Applied Research Clinical Genetics Clinical Diagnostic Tests   Learn more about our sophisticated, online genetic sample recruitment system. Online recruitment...

Gene Sciences & DNAjobs.com ... Jobs in Biotechnology, Pharmaceuticals, and
The Best Biotechnology, Medical, and Pharmaceutical Job Site on the Internet. Great resource for job seekers and recruiters....

GeneSage
GeneSage is dedicated to translating the promise of genomics into practical solutions for health professionals and consumers. In collaboration with distribution partners, GeneSage gives users a secure...

GenesRUs - National Newborn Screening and Genetics Resource Center
Quick Links GSB MCHB Technical Assistance Meeting for Newborn Screening & Genetics  Infrastructure Grants Newborn Screening: Characteristics of State Programs United States General Accounting Office ...

Genetic Alliance
Building partnerships to enhance the lives of everyone impacted by genetics...

Genetic Health Victoria
The clinics of Genetic Health Services Victoria are delivered through 10 metropolitan hospitals and 10 Rural and Regional Genetics Service centres....

Genetic Paternity Testing Professionals
Genetic Paternity Testing Professionals provides home paternity test kits or low cost legal results for use in court....

Genetic Science Learning Center
An educational resource that explains how genetics relates to our lives and society. Online activities, labs, and experiments for students, teachers and all others curious about genetics....

GeneTree Paternity Tests
Free home paternity collection kits for personal and AABB DNA services...

Genomic Disorders: mutation research, genetic disease
Mutation Research Centre...

Jesse's Journey - A Father's Tribute
Jesse's Journey - A Father's Tribute is the 1998 national campaign by Londoner John Davidson to create an endowment fund of ten million dollars for research to defeat a host of genetic diseases...

Journal of Medical Genetics
Journal of Medical Genetics...

Klinefelter Syndrome Support Group
Website for Klinefelter Syndrome support - By the late 1950s, researchers discovered that men with Klinefelter syndrome, as this group of symptoms came to be called, had an extra sex chromosome, XXY...

Mannosidosis - International Society for Mannosidosis & Related Diseases
A globally focused U.S. 501 c3 organization that advocates for persons affected by Oligosaccharide Storage Diseases...

MPS Society - The Society for Mucopolysaccharide Diseases
The Society for Mucopolysaccharide Disease - Information and support relating to MPS Diseases including Hunter, Morquio, Sanfilippo and Hurler....

myGeneticMD
myGeneticMD - Integrating Genetics into Healthy Living...

Myotubular Myopathy
Myotubular Myopathy (also called Centronuclear Myopathy) is a family of rare, inherited diseases....

National Ataxia Foundation
The National Ataxia Foundation is a nonprofit organization established in 1957 with the primary mission of encouraging and supporting research into Hereditary Ataxia, a group of neurological disorders...

National Foundation for Ectodermal Dysplasias
The National Foundation for Ectodermal Dysplasias (NFED) is committed to assisting people with ectodermal dysplasia to live not only normal life spans, but nearly normal life styles....

National Gaucher Foundation
Gaucher Disease is the most common lipid-storage disorder, and is the most common genetic disease affecting  Jewish people of Eastern European ancestry....

Neurofibromatosis resources
Support and information for those with Neurofibromatosis, Transcripts, Information, Links, A Bulletin Board, And Much, Much More! ...

NSGC
National Society of Genetic Counselors, Inc...

NSW Genetics Education Program
The NSW Genetics Education Program aims to provide information and resources relating to Genetics in Australia, in particular, genetic disorders, genetic counselling, testing, technology...

Our SMA Angels...
Dedicated to providing information and help for families facing the incurable genetic disease Spinal Muscular Atrophy (SMA) in their children. Come meet the kids, read their stories, see their faces....

Paternity DNA Testing By paternitytesters.com
Paternitytesters.com- Paternity Testing Laboratory offering AABB DNA Paternity Testing, Cheap Prices & Free DNA Banking Worldwide. For Confidential Results in 5 days, call 866-273-8323....

PhRMA Genomics: A Global Resource
. Bioterrorism News BSE Mad Cow News Last Update . 5 Sep 2024 As Reviewed by Genomics . Genomics Today - News updated every week day Genomics Lexicon - Terminology Definitions Genomics . ° Biodiversi...

PKD Foundation
The PKD Foundation web site. A site for profess, medical professionals, and researchers of the world's most common life-threatening genetic disease....

PKU Organization of Illinois
PKU Organization of Illinois Welcome to www.pkuil.org!  The purpose of this web site is to be a resource for families in Illinois and around the world dealing with Phenylketonuria....

Prader-Willi Alliance of New York
The Prader-Willi Alliance of New York, Inc. represents the interests of individuals in New York State with Prader-Willi syndrome, their families, and the professionals who provide services...

Prader-Willi Syndrome Association (UK)
Prader-Willi Syndrome (PWS) is a chromosomal disorder, which can affect people of both sexes and of any race or country. Three Swiss doctors -Prader, Labhart and Willi - first described it in 1956....

Pseudoxanthoma Elasticum (PXE)
PXE International, Inc. 4301 Connecticut Avenue, NW Suite 404 Washington, D.C. 20008-2304 Voice: 202.362.9599 Fax: 202.966.8553 e-mail - info@pxe.org...

Restless Legs Syndrome Foundation
provides information about RLS to patients and medical community regarding symptoms, and support resources...

Shwachman Diamond America
SDA is a non-profit organization which raises money for education of Shwachman-Diamond Syndrome...

Taryns world... and welcome to it
All about a genetic disease, called "Switches," including an online booklet by a mother about her son who has a rare disease called Hunter Syndrome...

The Cri du Chat Syndrome Support Group
The Cri du Chat Syndrome Support Group...

The Prader-Willi Syndrome Association (USA)
Prader-Willi Syndrome Association (USA) Homepage...

The Turner's Syndrome Society of the US
Learn about Turner syndrome, find medical information, order publications, share experiences, see some TS kids, and get screening information for TS....

Trisomy
S.O.F.T. is a nonprofit volunteer organization offering support for parents who have had a child with a chromesome disorder, and education to familes and professionals...

Tuberous Sclerosis Alliance
National Tuberous Sclerosis web site, for valuable information and support for those affected by tsc...

Tuberous Sclerosis Association, UK
The Tuberous Sclerosis Association, UK: Supporting sufferers, promoting awareness, and seeking the causes and best possible management of Tuberous Sclerosis....

Turner Syndrome, Its Symptoms and Treatments
Turner syndrome is one of the rare diseases that affect only girls. Short stature and a webbed neck are the most obvious signs of Turner Syndrome....

Von Hippel-Lindau (VHL) Family Alliance Home Page
Dedicated to improving diagnosis, treatment, and quality of life for individuals and families affected by von Hippel-Lindau disease....

Wide smiles
Cleft Lip and Palate Resource ...

XLH Network - Support Group for X-Linked Hypophosphatemia
We are a worldwide support organization for people living and dealing with X-Linked Hypophosphatemia (XLH) also known as Vitamin D-Resistant Rickets (VDRR). We are dedicated to understanding XLH...

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