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American Journal of Medical Genetics|August 10, 1999
Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literatureM Matsuo, K Muroya, K Kosaki, et al.American Journal of Medical Genetics|April 15, 2000
Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation: analysis of the X-inactivation patternsM Matsuo, K Muroya, K Nanao, et al.The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Micropenis and the AR Gene: mutation and CAG repeat-length analysisT Ishii, S Sato, K Kosaki, et al.Molecular Syndromology|November 4, 2010
Juvenile Muscular Atrophy of a Unilateral Upper Extremity (Hirayama Disease) in a Patient with CHARGE SyndromeT Yagihashi, K Hatori, K Ishii, et al.Pediatric Research|April 1, 1997
Parametric imaging of the chick embryonic cardiovascular system: a novel functional measureK Kosaki, H Suzuki, G W Schmid-Schönbein, et al.American Journal of Medical Genetics|January 24, 1998
Prader-Willi and Angelman syndromes: diagnosis with a bisulfite-treated methylation-specific PCR methodK Kosaki, M J McGinniss, A N Veraksa, et al.Pediatric Radiology|February 24, 2001
Spondylar dysplasia in type X collagenopathyG Nishimura, N Manabe, K Kosaki, et al.Molecular Psychiatry|March 13, 2001
Human homolog of the mouse imprinted gene Impact resides at the pericentric region of chromosome 18 within the critical region for bipolar affective disorderK Kosaki, T Suzuki, R Kosaki, et al.Clinical and Experimental Immunology|June 1, 1979
Pulmonary function changes in normal rats induced by antibody against rat IgEF B Casey, B E Abboa-OffeiCirculation|October 15, 1996
Failure to detect connexin43 mutations in 38 cases of sporadic and familial heterotaxyM Gebbia, J A Towbin, B CaseyPageof 24