Mechanisms of Disease: insights into X-linked and autosomal-dominant Kallmann syndrome
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Congenital Abnormalities - Kallmann Syndrome
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Extracellular Matrix Proteins
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Female Urogenital Diseases - Kallmann Syndrome
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Genes - Genes, X-Linked
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Genetic Diseases, Inborn - Kallmann Syndrome
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Gonadal Disorders - Kallmann Syndrome
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Humans
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Hypogonadism - Kallmann Syndrome
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Inheritance Patterns - Genes, X-Linked
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Male Urogenital Diseases - Kallmann Syndrome
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Mutation
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Nerve Tissue Proteins
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Phenotype
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Protein-Tyrosine Kinases - Receptor, Fibroblast Growth Factor, Type 1
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Receptors, Cell Surface - Receptor, Fibroblast Growth Factor, Type 1
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Receptors, Fibroblast Growth Factor - Receptor, Fibroblast Growth Factor, Type 1
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