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C I Kaye

Showing results (11-20 of 50) with videos related to

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The Journal of Laboratory and Clinical Medicine|September 1, 1975
Enzymic reduction of cystine and glutathione in cultivated human fibroblast from normal subjects and patients with cystinosisC I Kaye, H L Nadler
Journal of Craniofacial Genetics and Developmental Biology. Supplement|January 1, 1985
Hemifacial microsomia and the branchio-oto-renal syndromeB R Rollnick, C I Kaye
Birth Defects Original Article Series|January 1, 1975
Cutis laxa and associated anomaliesC I Kaye, D E Fisher
Anesthesia and Analgesia|October 1, 1991
Rumination risk of aspiration of gastric contents in the Prader-Willi syndromeT B Sloan, C I Kaye
American Journal of Medical Genetics|May 1, 1987
Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindredB R Rollnick, C I Kaye
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|January 1, 1974
Acid phosphatase isoenzymes in human skin fibroblastsC I Kaye, H L Nadler
American Journal of Medical Genetics|June 1, 1983
Hemifacial microsomia and variants: pedigree dataB R Rollnick, C I Kaye
The Journal of Pediatrics|April 1, 1982
Neonatal bromism secondary to maternal exposure in a photographic laboratoryH H Mangurten, C I Kaye
The Journal of Pediatrics|December 1, 1993
Membranous nephropathy in two human leukocyte antigen-identical brothersI Elshihabi, C I Kaye, A Brzowski
Archives of Dermatology|August 1, 1988
Autosomal recessive transmission of neuroectodermal syndromeJ Zunich, N B Esterly, C I Kaye
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
The Journal of Laboratory and Clinical Medicine|September 1, 1975
Enzymic reduction of cystine and glutathione in cultivated human fibroblast from normal subjects and patients with cystinosisC I Kaye, H L Nadler
Journal of Craniofacial Genetics and Developmental Biology. Supplement|January 1, 1985
Hemifacial microsomia and the branchio-oto-renal syndromeB R Rollnick, C I Kaye
Birth Defects Original Article Series|January 1, 1975
Cutis laxa and associated anomaliesC I Kaye, D E Fisher
Anesthesia and Analgesia|October 1, 1991
Rumination risk of aspiration of gastric contents in the Prader-Willi syndromeT B Sloan, C I Kaye
American Journal of Medical Genetics|May 1, 1987
Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindredB R Rollnick, C I Kaye
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|January 1, 1974
Acid phosphatase isoenzymes in human skin fibroblastsC I Kaye, H L Nadler
American Journal of Medical Genetics|June 1, 1983
Hemifacial microsomia and variants: pedigree dataB R Rollnick, C I Kaye
The Journal of Pediatrics|April 1, 1982
Neonatal bromism secondary to maternal exposure in a photographic laboratoryH H Mangurten, C I Kaye
The Journal of Pediatrics|December 1, 1993
Membranous nephropathy in two human leukocyte antigen-identical brothersI Elshihabi, C I Kaye, A Brzowski
Archives of Dermatology|August 1, 1988
Autosomal recessive transmission of neuroectodermal syndromeJ Zunich, N B Esterly, C I Kaye
Pageof 5