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M Opitz

Showing results (411-420 of 520) with videos related to

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European Journal of Pediatrics|August 16, 1976
A severe infantile micromelic chondrodysplasia which resembles Kniest diseaseL O Langer, M Gonzalez-Ramos, H Chen, et al.
Pathology Annual|January 1, 1987
Pathologic changes of osteochondrodysplasia in infancy. A reviewE F Gilbert, S S Yang, L Langer, et al.
Clinical Dysmorphology|June 3, 2005
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndromeElisabetta Tabolacci, Marcella Zollino, Rosetta Lecce, et al.
Avian Diseases|April 1, 1992
Molecular characterization of Salmonella enteritidis isolates from Maine poultry and poultry farm environmentsJ T Singer, H M Opitz, M Gershman, et al.
Clinical Genetics|November 1, 1976
Hypertrichosis lanuginosa in a mother and sonN Freire-Maia, J Felizali, A C de Figueiredo, et al.
Nuclear Medicine Communications|March 16, 2000
67Ga-citrate and 99Tcm-MDP for estimating the severity of vertebral osteomyelitisS Gratz, J Dörner, J W Oestmann, et al.
Fetal and Pediatric Pathology|March 17, 2005
Probable second fetus with Marles-Chudley syndrome: cardiac calcifications with ulnar deficiency and absent/hypoplastic thumbsDavid A Wada, Juliana Szakacs, Anne M Kennedy, 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|January 11, 1976
Essential tremor, nystagmus and duodenal ulceration. A "new" dominantly inherited conditionG Neuhäuser, R F Daly, N C Magnelli, et al.
Pageof 52

Showing results (411-420 of 520) with videos related to

Sort By:
Pageof 52
European Journal of Pediatrics|August 16, 1976
A severe infantile micromelic chondrodysplasia which resembles Kniest diseaseL O Langer, M Gonzalez-Ramos, H Chen, et al.
Pathology Annual|January 1, 1987
Pathologic changes of osteochondrodysplasia in infancy. A reviewE F Gilbert, S S Yang, L Langer, et al.
Clinical Dysmorphology|June 3, 2005
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndromeElisabetta Tabolacci, Marcella Zollino, Rosetta Lecce, et al.
Avian Diseases|April 1, 1992
Molecular characterization of Salmonella enteritidis isolates from Maine poultry and poultry farm environmentsJ T Singer, H M Opitz, M Gershman, et al.
Clinical Genetics|November 1, 1976
Hypertrichosis lanuginosa in a mother and sonN Freire-Maia, J Felizali, A C de Figueiredo, et al.
Nuclear Medicine Communications|March 16, 2000
67Ga-citrate and 99Tcm-MDP for estimating the severity of vertebral osteomyelitisS Gratz, J Dörner, J W Oestmann, et al.
Fetal and Pediatric Pathology|March 17, 2005
Probable second fetus with Marles-Chudley syndrome: cardiac calcifications with ulnar deficiency and absent/hypoplastic thumbsDavid A Wada, Juliana Szakacs, Anne M Kennedy, 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|January 11, 1976
Essential tremor, nystagmus and duodenal ulceration. A "new" dominantly inherited conditionG Neuhäuser, R F Daly, N C Magnelli, et al.
Pageof 52