Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH. (Q50802025)
scientific article published on 12 June 2012
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| English | Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH. |
scientific article published on 12 June 2012 |
Statements
Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH. (English)
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Joe Rainger
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Hemant Bengani
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Leigh Campbell
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Eve Anderson
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Kishan Sokhi
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Wayne Lam
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Angelika Riess
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Morad Ansari
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Sarah Smithson
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Melissa Lees
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Catherine Mercer
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Kathryn McKenzie
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Tobias Lengfeld
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Blanca Gener Querol
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Peter Branney
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Stewart McKay
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Harris Morrison
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Bethan Medina
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Morag Robertson
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Jürgen Kohlhase
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Colin Gordon
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Jean Kirk
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Dagmar Wieczorek
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12 June 2012
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21
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18
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3969-3983
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Identifiers
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