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C O Leonard

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

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The Journal of Pediatrics|August 1, 1988
Natural history of Williams syndrome: physical characteristicsC A Morris, S A Demsey, C O Leonard, et al.
The Journal of Clinical Ethics|January 1, 1991
The effect of education on physicians' knowledge of a laboratory test: the case of maternal serum alpha-fetoprotein screeningN A Holtzman, R R Faden, C O Leonard, et al.
Advances in Experimental Medicine and Biology|January 1, 1972
Further studies on the antenatal detection of sickle cell anemia and other hemoglobinopathiesH H Kazazian, M M Kaback, A P Woodhead, et al.
American Journal of Public Health|December 1, 1985
What participants understand about a maternal serum alpha-fetoprotein screening programR R Faden, A J Chwalow, E Orel-Crosby, et al.
The Johns Hopkins Medical Journal|October 1, 1979
Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8G S Pai, G H Thomas, C O Leonard, et al.
American Journal of Medical Genetics|December 8, 1998
Pituitary macroadenoma and cranial osteoma in a manifesting heterozygote with the Opitz G/BBB syndromeJ K Brooks, C O Leonard, J K Zawadzki, et al.
Social Biology|January 1, 1986
Assessment of risk by pregnant women: implications for genetic counseling and educationG A Chase, R R Faden, N A Holtzman, et al.
American Journal of Public Health|March 1, 1987
Prenatal screening and pregnant women's attitudes toward the abortion of defective fetusesR R Faden, A J Chwalow, K Quaid, et al.
The Journal of Pediatrics|April 1, 1989
Prenatal diagnosis and heterozygote detection by DNA analysis in ornithine transcarbamylase deficiencyJ E Spence, A Maddalena, W E O'Brien, et al.
American Journal of Medical Genetics|February 6, 1999
Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: the M syndromeA Rauch, K A Feindt, C O Leonard, et al.
Pageof 4

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

Sort By:
Pageof 4
The Journal of Pediatrics|August 1, 1988
Natural history of Williams syndrome: physical characteristicsC A Morris, S A Demsey, C O Leonard, et al.
The Journal of Clinical Ethics|January 1, 1991
The effect of education on physicians' knowledge of a laboratory test: the case of maternal serum alpha-fetoprotein screeningN A Holtzman, R R Faden, C O Leonard, et al.
Advances in Experimental Medicine and Biology|January 1, 1972
Further studies on the antenatal detection of sickle cell anemia and other hemoglobinopathiesH H Kazazian, M M Kaback, A P Woodhead, et al.
American Journal of Public Health|December 1, 1985
What participants understand about a maternal serum alpha-fetoprotein screening programR R Faden, A J Chwalow, E Orel-Crosby, et al.
The Johns Hopkins Medical Journal|October 1, 1979
Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8G S Pai, G H Thomas, C O Leonard, et al.
American Journal of Medical Genetics|December 8, 1998
Pituitary macroadenoma and cranial osteoma in a manifesting heterozygote with the Opitz G/BBB syndromeJ K Brooks, C O Leonard, J K Zawadzki, et al.
Social Biology|January 1, 1986
Assessment of risk by pregnant women: implications for genetic counseling and educationG A Chase, R R Faden, N A Holtzman, et al.
American Journal of Public Health|March 1, 1987
Prenatal screening and pregnant women's attitudes toward the abortion of defective fetusesR R Faden, A J Chwalow, K Quaid, et al.
The Journal of Pediatrics|April 1, 1989
Prenatal diagnosis and heterozygote detection by DNA analysis in ornithine transcarbamylase deficiencyJ E Spence, A Maddalena, W E O'Brien, et al.
American Journal of Medical Genetics|February 6, 1999
Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: the M syndromeA Rauch, K A Feindt, C O Leonard, et al.
Pageof 4