PubMed MeSh Term
RDF
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Genetic Diseases, Inborn - Dwarfism
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Genetic Diseases, Inborn - Dyskeratosis Congenita
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Genetic Diseases, Inborn - Ehlers-Danlos Syndrome
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Genetic Diseases, Inborn - Epidermolysis Bullosa, Junctional
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Genetic Diseases, Inborn - Eye Diseases, Hereditary
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Genetic Diseases, Inborn - Fragile X Syndrome
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Genetic Diseases, Inborn - Fragile X Syndrome
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Genetic Diseases, Inborn - Friedreich Ataxia
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Genetic Diseases, Inborn - Gangliosidosis, GM1
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Genetic Diseases, Inborn - Gangliosidosis, GM1
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Genetic Diseases, Inborn - Gangliosidosis, GM1
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Genetic Diseases, Inborn - Gaucher Disease
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Genetic Diseases, Inborn - Gaucher Disease
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Genetic Diseases, Inborn - Gaucher Disease
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Genetic Diseases, Inborn - Hermanski-Pudlak Syndrome
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Genetic Diseases, Inborn - Hermanski-Pudlak Syndrome
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Genetic Diseases, Inborn - Hermanski-Pudlak Syndrome
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Genetic Diseases, Inborn - Hermanski-Pudlak Syndrome
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Genetic Diseases, Inborn - Holoprosencephaly
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Genetic Diseases, Inborn - Huntington Disease
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Genetic Diseases, Inborn - Ichthyosis, Lamellar
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Genetic Diseases, Inborn - Kallmann Syndrome
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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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