Results 1 -
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34
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"X-linked" dominant inheritance
- Immune System and Disorders/Specifics ... Immune System and Disorders ... NIAID researches congenital neutropenia syndromes, a group of rare disorders present from ...
- Newborn Screening/Reference Desk ... Newborn Screening ... Genetic Testing/Reference Desk ... Genetic Testing ... National Center for Biotechnology Information ... From the National ...
- Nystagmus (American Association for Pediatric Ophthalmology and Strabismus)Eye Movement Disorders/Start Here ... Eye Movement Disorders ... GLOSSARY, TERMS, ACRONYMS, PHRASES, DEFINITIONS, DICTIONARY ... Shows a single glossary entry ... American ...
- Genetics and Neuromuscular Disease (Muscular Dystrophy Association) - PDFNeuromuscular Disorders/Genetics ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF
- Retinitis Pigmentosa (Foundation Fighting Blindness)Usher Syndrome/Learn More ... Usher Syndrome ... Retinal Disorders/Specifics ... Retinal Disorders ... Foundation Fighting Blindness ... What is Retinitis Pigmentosa? Learn about ...
- Fragile X Syndrome/Start Here ... Fragile X Syndrome ... National Human Genome Research Institute ... From the National Institutes of Health ... Fragile X syndrome is an ...
- Causes of Charcot-Marie-Tooth Disease (CMT) (Muscular Dystrophy Association)MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.
- Resources about some of the forms of primary immune deficiency diseases (PIDDs) which NIAID is currently studying. ... Immune System and Disorders/Specifics ...
- Immune System and Disorders/Specifics ... Immune System and Disorders ... NIAID studies XLA, an inherited immune disorder caused by an inability to produce B cells ...
- Immune System and Disorders/Specifics ... Immune System and Disorders ... DOCK8 deficiency is a rare immune disorder named after the mutated gene which NIAID scientists ...