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J M Opitz

Showing results (281-290 of 338) with videos related to

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Pathology Annual|January 1, 1987
Pathologic changes of osteochondrodysplasia in infancy. A reviewE F Gilbert, S S Yang, L Langer, et al.
Clinical Genetics|January 11, 1976
Essential tremor, nystagmus and duodenal ulceration. A "new" dominantly inherited conditionG Neuhäuser, R F Daly, N C Magnelli, 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 Medical Genetics|January 1, 1980
Multiple pterygium syndromeH Chen, C H Chang, R P Misra, et al.
The American Journal of Medicine|December 1, 1970
Familial thrombocytopenia, elevated serum IgA levels and renal disease. A report of a kindredJ Gutenberger, C W Trygstad, E R Stiehm, et al.
Clinical Genetics|November 1, 1976
Hypertrichosis lanuginosa in a mother and sonN Freire-Maia, J Felizali, A C de Figueiredo, et al.
Journal of Medical Genetics|September 1, 1975
A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signsN Freire-Maia, V A Fortes, L C Pereira, et al.
American Journal of Medical Genetics|January 1, 1983
Renal failure with hypercalcemia, renal stones, multiple pathologic fractures, and growth failureR W Chesney, A L Friedman, A L Breed, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1983
Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa functionS Pang, L S Levine, E Stoner, et al.
American Journal of Medical Genetics|January 1, 1982
Clinicopathologic conference: a six-month-old infant with sudden onset of metabolic acidosis and shockM L Katcher, W E Segar, J J Wolfson, et al.
Pageof 34

Showing results (281-290 of 338) with videos related to

Sort By:
Pageof 34
Pathology Annual|January 1, 1987
Pathologic changes of osteochondrodysplasia in infancy. A reviewE F Gilbert, S S Yang, L Langer, et al.
Clinical Genetics|January 11, 1976
Essential tremor, nystagmus and duodenal ulceration. A "new" dominantly inherited conditionG Neuhäuser, R F Daly, N C Magnelli, 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 Medical Genetics|January 1, 1980
Multiple pterygium syndromeH Chen, C H Chang, R P Misra, et al.
The American Journal of Medicine|December 1, 1970
Familial thrombocytopenia, elevated serum IgA levels and renal disease. A report of a kindredJ Gutenberger, C W Trygstad, E R Stiehm, et al.
Clinical Genetics|November 1, 1976
Hypertrichosis lanuginosa in a mother and sonN Freire-Maia, J Felizali, A C de Figueiredo, et al.
Journal of Medical Genetics|September 1, 1975
A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signsN Freire-Maia, V A Fortes, L C Pereira, et al.
American Journal of Medical Genetics|January 1, 1983
Renal failure with hypercalcemia, renal stones, multiple pathologic fractures, and growth failureR W Chesney, A L Friedman, A L Breed, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1983
Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa functionS Pang, L S Levine, E Stoner, et al.
American Journal of Medical Genetics|January 1, 1982
Clinicopathologic conference: a six-month-old infant with sudden onset of metabolic acidosis and shockM L Katcher, W E Segar, J J Wolfson, et al.
Pageof 34