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Endocrinologia Japonica|April 1, 1991
Silent thyroiditis in an eleven-year-old girl, associated with transient increase in serum IgM and thyroid hormoneM Masuno, J Kosaka, S NakamuraResearch Communications in Chemical Pathology and Pharmacology|September 1, 1980
No enhanced elimination of propranolol in patients with hyperthyroidismT Ishizaki, M Masuno, K TawaraActa Paediatrica Japonica : Overseas Edition|April 1, 1989
Restriction fragment length polymorphism analysis in healthy Japanese individuals and Japanese families with Gaucher diseaseM Masuno, T Orii, K Sukegawa, et al.American Journal of Medical Genetics|June 1, 1994
Epidemiology of limb-body wall complex in JapanK Kurosawa, K Imaizumi, M Masuno, et al.Human Genetics|January 1, 1990
Non-existence of a tight association between a 444leucine to proline mutation and phenotypes of Gaucher disease: high frequency of a NciI polymorphism in the non-neuronopathic formM Masuno, S Tomatsu, K Sukegawa, et al.Clinical Dysmorphology|August 5, 1998
Association of holoprosencephaly, ectrodactyly, cleft lip/cleft palate and hypertelorism: a possible third caseK Imaizumi, T Ishii, M Masuno, et al.American Journal of Medical Genetics|December 14, 1999
Apple-peel intestinal atresia associated with balanced reciprocal translocation t(2;3)(q31.3;p24.2) matK Imaizumi, J Kimura, M Masuno, et al.Clinical Genetics|January 1, 1994
Male with type II autosomal recessive cutis laxaK Imaizumi, K Kurosawa, Y Makita, et al.American Journal of Medical Genetics|October 23, 1995
Hypoglycemia in Coffin-Siris syndromeK Imaizumi, M Nakamura, M Masuno, et al.American Journal of Medical Genetics|May 22, 1995
Autosomal dominant inheritance in Setleis syndromeM Masuno, K Imaizumi, Y Makita, et al.Pageof 6