Cockayne Syndrome
Cockayne syndrome is a rare autosomal recessive disease of complex clinical phenotype that usually presents in early childhood. Characteristically the child presents with delayed milestones, growth and mental retardation associated with typical facies, photosensitivity, retinitis pigmentosa, deafnes...
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Huvudskapare: | , , , |
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Materialtyp: | Bok |
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Wolters Kluwer Medknow Publications,
2003-01-01T00:00:00Z.
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Internet
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A1234.567 |
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Exemplar 1 | Tillgänglig |