(Q51915083)
Statements
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A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity. (English)
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Monica C Varela
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Alex Y Simões-Sato
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Claudia I E De Castro
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Celia P Koiffmann
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4 January 2006
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49
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4
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298-305
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Identifiers
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