Worldwide support network for people who care about people with alagille syndrome.
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works to establish minimum standards of practice, to encourage professional growth, and to increase recognition of the genetic counselling profession in Canada.
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international not-for-profit organization dedicated to educating and bringing together families with children who have Alfi's syndrome.
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Official site of the International Costello Syndrome Support Group. Includes medical information, photographs and videos, therapy ideas, news, and links.
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Informational site provides details on newborn screening, on numerous diseases, medical information and support resources such as a newsletter and email List.
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Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients.
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provides a global resource for genetics information including a directory of condition-specific lay advocacy member groups.
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offers general information on conditions, DNA mutations, genetic testing, and research participation.
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national U.K. alliance of organizations which support children, families, and individuals affected by genetic disorders and genetic diseases.
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A non profit Organization dedicated to those families that are touched by a rare blood disease known as Hereditary Angioedema
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nonprofit, basic science organization dedicated to the cure of genetic disease.
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The IMMD is a genetic testing laboratory located in Germany. Provides genetic tests for hereditary breast cancer, various cardiovascular diseases or diseases with onset in childhood.
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Offers education, medical referrals, up-dates, and support to all individuals interested in Machado-Joseph Disease.
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Organization, conferences and contact details. FAQs about the disease, information center and resources.
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Fully accessible site for people with LMBB, their families, friends, carers and interested professionals. Opinions, news, views, research, updates, and contact details.
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information forum on ML$, a rare genetic disease.
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The home page of Nail-Patella Syndrome Worldwide, the only non-profit serving the needs of people with Nail-Patella Syndrome. Includes information on the syndrome and the work of the organization.
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information and support for this rare chromosomal disorder.
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Support and education for families and professionals. Includes abstracts, brochures, glossary, links and newsletters.
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The comprehensive source for pseudoxanthoma elasticum research and world wide activities.
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