Results 1 -
8
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8
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autosomal
- Genetics and Neuromuscular Disease (Muscular Dystrophy Association) - PDFNeuromuscular Disorders/Genetics ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF
- Diagnosed with NF2-Related Schwannomatosis (Children's Tumor Foundation) - PDFNeurofibromatosis/Specifics ... Neurofibromatosis ... Children's Tumor Foundation ... PDF
- Hereditary Pancreatitis (National Pancreas Foundation) - PDFPancreatitis/Genetics ... Pancreatitis ... National Pancreas Foundation ... PDF ... HEREDITARY PANCREATITIS | FAMILIAL PANCREATITIS | GENETIC TESTING | PATIENT STORY | RESOURCES ...
- Hypophosphatasia (Osteogenesis Imperfecta Foundation) - PDFBone Diseases/Specifics ... Bone Diseases ... Osteogenesis Imperfecta/Related Issues ... Osteogenesis Imperfecta ... Osteogenesis Imperfecta Foundation ... PDF
- Physical Therapy for Facioscapulohumeral Muscular Dystrophy (FSHD) (FacioScapuloHumeral Muscular Dystrophy Society) - PDFMuscular Dystrophy/Living With ... Muscular Dystrophy ... FacioScapuloHumeral Muscular Dystrophy Society ... PDF
- Ehlers-Danlos Syndrome Hypermobility Type (Marfan Foundation) - PDFEhlers-Danlos Syndrome/Learn More ... Ehlers-Danlos Syndrome ... Marfan Foundation ... PDF
- Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDFNeuromuscular Disorders/Living With ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF ... muscular dystrophy; exercise with a disability; neuromuscular ...
- Guide to Understanding Pfeiffer Syndrome (Children's Craniofacial Association) - PDFCraniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF