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G Kohn

Showing results (161-170 of 193) with videos related to

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JAMA|October 23, 1981
XX/XY lymphoid chimerism in a boy with fatal lymphohistiocytic proliferationG Cividalli, S Yatziv, R Voss, et al.
Journal of Medical Genetics|November 1, 1992
Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophyJ Myring, A L Meredith, H G Harley, et al.
Journal of the American Dental Association (1939)|February 13, 2004
Guidelines for infection control in dental health care settings--2003William G Kohn, Jennifer A Harte, Dolores M Malvitz, et al.
MMWR. Recommendations and Reports : Morbidity and Mortality Weekly Report. Recommendations and Reports|December 20, 2003
Guidelines for infection control in dental health-care settings--2003William G Kohn, Amy S Collins, Jennifer L Cleveland, et al.
Acta Endocrinologica|June 1, 1986
Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase deficiency: gender reassignment in early infancyD J Gross, H Landau, G Kohn, et al.
Clinical Genetics|September 1, 1981
Prenatal diagnosis of Fanconi anemiaR Voss, G Kohn, M Shaham, et al.
Pediatric Research|October 1, 1978
A new variant of mannosidosis with increased residual enzymatic activity and mild clinical manifestationG Bach, G Kohn, E E Lasch, et al.
The Journal of Innovations in Cardiac Rhythm Management|June 2, 2020
Wearable Cardioverter-defibrillators for the Prevention of Sudden Cardiac Death: A Meta-analysisElaine Nguyen, Erin R Weeda, Christine G Kohn, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|August 10, 2018
External validation of three risk stratification rules in patients presenting with pulmonary embolism and cancerErin R Weeda, Jonathan T Caranfa, Gary H Lyman, et al.
Prenatal Diagnosis|August 1, 1990
Congenital hereditary hypothyroidism--prenatal diagnosis and treatmentM Hirsch, Z Josefsberg, A Schoenfeld, et al.
Pageof 20

Showing results (161-170 of 193) with videos related to

Sort By:
Pageof 20
JAMA|October 23, 1981
XX/XY lymphoid chimerism in a boy with fatal lymphohistiocytic proliferationG Cividalli, S Yatziv, R Voss, et al.
Journal of Medical Genetics|November 1, 1992
Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophyJ Myring, A L Meredith, H G Harley, et al.
Journal of the American Dental Association (1939)|February 13, 2004
Guidelines for infection control in dental health care settings--2003William G Kohn, Jennifer A Harte, Dolores M Malvitz, et al.
MMWR. Recommendations and Reports : Morbidity and Mortality Weekly Report. Recommendations and Reports|December 20, 2003
Guidelines for infection control in dental health-care settings--2003William G Kohn, Amy S Collins, Jennifer L Cleveland, et al.
Acta Endocrinologica|June 1, 1986
Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase deficiency: gender reassignment in early infancyD J Gross, H Landau, G Kohn, et al.
Clinical Genetics|September 1, 1981
Prenatal diagnosis of Fanconi anemiaR Voss, G Kohn, M Shaham, et al.
Pediatric Research|October 1, 1978
A new variant of mannosidosis with increased residual enzymatic activity and mild clinical manifestationG Bach, G Kohn, E E Lasch, et al.
The Journal of Innovations in Cardiac Rhythm Management|June 2, 2020
Wearable Cardioverter-defibrillators for the Prevention of Sudden Cardiac Death: A Meta-analysisElaine Nguyen, Erin R Weeda, Christine G Kohn, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|August 10, 2018
External validation of three risk stratification rules in patients presenting with pulmonary embolism and cancerErin R Weeda, Jonathan T Caranfa, Gary H Lyman, et al.
Prenatal Diagnosis|August 1, 1990
Congenital hereditary hypothyroidism--prenatal diagnosis and treatmentM Hirsch, Z Josefsberg, A Schoenfeld, et al.
Pageof 20