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Autosomal recessive mental retardation%25252C deafness%25252…
Autosomal recessive mental retardation%25252C deafness%25252C ankylosis%25252C and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family
Autosomal recessive mental retardation%25252C deafness%25252C ankylosis%25252C and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family
Article, Chapter
Authors: E. Morava
Publication: Journal of Clinical Endocrinology and Metabolism, The, Volume:96, Issue:1, Page(s):E189
Published: 2011
ISSN: 0021-972X
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View Full Text Source:Journal of Clinical Endocrinology and Metabolism, The,Journal of Clinical Endocrinology and Metabolism, The,Oxford University Press Journals (UKB 2021-2023) Opens in new Window
Journal:  Journal of Clinical Endocrinology and Metabolism, The Source:Oxford University Press Journals (UKB 2021-2023) Opens in new Window
Collection:  Oxford University Press Journals (UKB 2021-2023)
Coverage:
  • 1996~present; volume:81~present;issue:1~present
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