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Osteoporosis, Fractures, and Blindness Due to a Missense Mutation in the LRP5 Receptor by Littman J, Phornphutkul C, Saade C, Katarincic J, Aaron R
Published 2023-03-01
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Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy. by Sagen, J, Raeder, H, Hathout, E, Shehadeh, N, Gudmundsson, K, Baevre, H, Abuelo, D, Phornphutkul, C, Molnes, J, Bell, G, Gloyn, A, Hattersley, A, Molven, A, Søvik, O, Njølstad, P
Published 2004Journal article