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The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
Medical genetics in ThailandC SirinavinJournal of Medical Genetics|December 1, 1975
Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literatureC Sirinavin, A A TrowbridgeClinical Genetics|August 1, 1982
Digital clubbing, hyperhidrosis, acro-osteolysis and osteoporosis. A case resembling pachydermoperiostosisC Sirinavin, N R Buist, P MokkhavesAmerican Journal of Hematology|January 1, 1977
Dyskeratosis congenita: hematologic evaluation of a sibship and review of the literatureA A Trowbridge, C Sirinavin, J W LinmanJournal of the Medical Association of Thailand = Chotmaihet Thangphaet|January 22, 2002
Molecular defect of PKD1 gene resulting in abnormal RNA processing in a Thai familyN Rungroj, W Thongnoppakhun, K Vareesangthip, et al.Human Mutation|December 29, 1999
A novel splice-acceptor site mutation (IVS13-2A>T) of polycystic kidney disease 1 (PKD1) gene resulting in an RNA processing defect with a 74-nucleotide deletion in exon 14 of the mRNA transcriptA Thongnoppakhun, N Rungroj, P Wilairat, et al.Human Molecular Genetics|January 1, 1994
Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locusR Twells, P T Yenchitsomanus, C Sirinavin, et al.Pageof 1