PubMed MeSh Term
RDF
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Genetic Diseases, Inborn - Kartagener Syndrome
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Genetic Diseases, Inborn - Kartagener Syndrome
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Genetic Diseases, Inborn - Keratoderma, Palmoplantar
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Genetic Diseases, Inborn - Maple Syrup Urine Disease
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Genetic Diseases, Inborn - Maple Syrup Urine Disease
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Genetic Diseases, Inborn - Mental Retardation, X-Linked
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Genetic Diseases, Inborn - Metabolism, Inborn Errors
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Genetic Diseases, Inborn - Metal Metabolism, Inborn Errors
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Genetic Diseases, Inborn - Muscular Dystrophies
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Genetic Diseases, Inborn - Muscular Dystrophy, Duchenne
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Genetic Diseases, Inborn - Muscular Dystrophy, Facioscapulohumeral
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Genetic Diseases, Inborn - Neurofibromatosis 1
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Genetic Diseases, Inborn - Neurofibromatosis 1
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Genetic Diseases, Inborn - Osteochondrodysplasias
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Genetic Diseases, Inborn - Peroxisomal Disorders
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Genetic Diseases, Inborn - Phenylketonurias
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Genetic Diseases, Inborn - Phenylketonurias
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Genetic Diseases, Inborn - Primary Immunodeficiency Diseases
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Genetic Diseases, Inborn - Progeria
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Genetic Diseases, Inborn - Purine-Pyrimidine Metabolism, Inborn Errors
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Genetic Diseases, Inborn - Retinitis Pigmentosa
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Genetic Diseases, Inborn - Severe Combined Immunodeficiency
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Genetic Diseases, Inborn - Smith-Magenis Syndrome
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Genetic Diseases, Inborn - Spinocerebellar Ataxias
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Genetic Diseases, Inborn - Tuberous Sclerosis
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Genetic Diseases, Inborn - Tuberous Sclerosis
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Genetic Diseases, Inborn - Walker-Warburg Syndrome
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Genetic Diseases, Inborn - Werner Syndrome
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Genetic Diseases, Inborn - Wiskott-Aldrich Syndrome
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Genetic Diseases, Inborn - Wiskott-Aldrich Syndrome
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