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C Viseskul

Showing results (21-30 of 35) with videos related to

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Archives of Pathology & Laboratory Medicine|April 1, 1977
Sudden infant death due to congenital adrenal hypoplasiaM A Russell, J M Opitz, C Viseskul, et al.
Zeitschrift Fur Kinderheilkunde|August 31, 1973
Familial bilateral renal agenesis and hereditary renal adysplasiaR M Buchta, C Viseskul, E F Gilbert, et al.
American Journal of Medical Genetics|January 1, 1980
Clinicopathologic conference: a three-month-old infant with failure to thrive, hepatomegaly, and neurological impairmentA Friedman, J Bethzhold, R Hong, et al.
Acta Neuropathologica|December 3, 1973
Minamata disease. A case report and a comparative studyL W Chang, J M Opitz, P D Pallister, et al.
Birth Defects Original Article Series|January 1, 1974
Pathology of chondrodysplasia punctata rhizomelic typeC Viseskul, J M Opitz, J W Spranger, et al.
European Journal of Pediatrics|October 1, 1976
Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 casesA L Kosseff, J Herrmann, E F Gilbert, et al.
European Journal of Pediatrics|August 1, 1980
A fetus with upper limb amelia, "caudal regression" and Dandy-Walker defect with an insulin-dependent diabetic motherH J Bruyere, C Viseskul, J M Opitz, et al.
European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.
American Journal of Diseases of Children (1960)|July 1, 1978
Myocardial infarct in a child with systemic lupus erythematosusS Ishikawa, W E Segar, E F Gilbert, et al.
Archives of Pathology & Laboratory Medicine|October 1, 1990
Neonatal intracranial choriocarcinomaS A Chandra, E F Gilbert, C Viseskul, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Archives of Pathology & Laboratory Medicine|April 1, 1977
Sudden infant death due to congenital adrenal hypoplasiaM A Russell, J M Opitz, C Viseskul, et al.
Zeitschrift Fur Kinderheilkunde|August 31, 1973
Familial bilateral renal agenesis and hereditary renal adysplasiaR M Buchta, C Viseskul, E F Gilbert, et al.
American Journal of Medical Genetics|January 1, 1980
Clinicopathologic conference: a three-month-old infant with failure to thrive, hepatomegaly, and neurological impairmentA Friedman, J Bethzhold, R Hong, et al.
Acta Neuropathologica|December 3, 1973
Minamata disease. A case report and a comparative studyL W Chang, J M Opitz, P D Pallister, et al.
Birth Defects Original Article Series|January 1, 1974
Pathology of chondrodysplasia punctata rhizomelic typeC Viseskul, J M Opitz, J W Spranger, et al.
European Journal of Pediatrics|October 1, 1976
Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 casesA L Kosseff, J Herrmann, E F Gilbert, et al.
European Journal of Pediatrics|August 1, 1980
A fetus with upper limb amelia, "caudal regression" and Dandy-Walker defect with an insulin-dependent diabetic motherH J Bruyere, C Viseskul, J M Opitz, et al.
European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.
American Journal of Diseases of Children (1960)|July 1, 1978
Myocardial infarct in a child with systemic lupus erythematosusS Ishikawa, W E Segar, E F Gilbert, et al.
Archives of Pathology & Laboratory Medicine|October 1, 1990
Neonatal intracranial choriocarcinomaS A Chandra, E F Gilbert, C Viseskul, et al.
Pageof 4