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S Malcolm

Showing results (111-120 of 271) with videos related to

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American Journal of Medical Genetics|January 2, 1995
Proportions of spontaneous mutations in males and females with ornithine transcarbamylase deficiencyM Tuchman, I Matsuda, A Munnich, et al.
Human Genetics|February 1, 1992
Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndromeJ C Smith, T Webb, M E Pembrey, et al.
Bone Marrow Transplantation|March 1, 1990
The use of locus-specific minisatellite probes to check engraftment following allogeneic bone marrow transplantation for severe combined immunodeficiency diseaseF Katz, S Malcolm, S Strobel, et al.
Archives of Disease in Childhood|August 1, 1989
Absence of Y specific DNA sequences in two siblings with 46XX hermaphroditismJ Raine, M E Robertson, S Malcolm, et al.
Blood|August 15, 1990
RFLP and deletion analysis for X-linked chronic granulomatous disease using the cDNA probe: potential for improved prenatal diagnosis and carrier determinationA Pelham, M A O'Reilly, S Malcolm, et al.
Southern Medical Journal|November 1, 1978
Hepatic hemangioendotheliomas and hyperbilirubinemiaG G Smith, J A Lohr, B S Malcolm, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|April 24, 2007
Directed disassembly of an interfacial rubisco protein networkSagheer A Onaizi, Andrew S Malcolm, Lizhong He, et al.
American Journal of Human Genetics|April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndromeK Buiting, A Barnicoat, C Lich, et al.
Molecular and Cellular Biology|March 18, 2003
Dissecting the contribution of p16(INK4A) and the Rb family to the Ras transformed phenotypePhilip J Mitchell, Elena Perez-Nadales, Denise S Malcolm, et al.
Infection Control and Hospital Epidemiology|December 1, 1995
Contaminated foods in healthcare facilitiesS Brooks, S Malcolm, P Lamont, et al.
Pageof 28

Showing results (111-120 of 271) with videos related to

Sort By:
Pageof 28
American Journal of Medical Genetics|January 2, 1995
Proportions of spontaneous mutations in males and females with ornithine transcarbamylase deficiencyM Tuchman, I Matsuda, A Munnich, et al.
Human Genetics|February 1, 1992
Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndromeJ C Smith, T Webb, M E Pembrey, et al.
Bone Marrow Transplantation|March 1, 1990
The use of locus-specific minisatellite probes to check engraftment following allogeneic bone marrow transplantation for severe combined immunodeficiency diseaseF Katz, S Malcolm, S Strobel, et al.
Archives of Disease in Childhood|August 1, 1989
Absence of Y specific DNA sequences in two siblings with 46XX hermaphroditismJ Raine, M E Robertson, S Malcolm, et al.
Blood|August 15, 1990
RFLP and deletion analysis for X-linked chronic granulomatous disease using the cDNA probe: potential for improved prenatal diagnosis and carrier determinationA Pelham, M A O'Reilly, S Malcolm, et al.
Southern Medical Journal|November 1, 1978
Hepatic hemangioendotheliomas and hyperbilirubinemiaG G Smith, J A Lohr, B S Malcolm, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|April 24, 2007
Directed disassembly of an interfacial rubisco protein networkSagheer A Onaizi, Andrew S Malcolm, Lizhong He, et al.
American Journal of Human Genetics|April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndromeK Buiting, A Barnicoat, C Lich, et al.
Molecular and Cellular Biology|March 18, 2003
Dissecting the contribution of p16(INK4A) and the Rb family to the Ras transformed phenotypePhilip J Mitchell, Elena Perez-Nadales, Denise S Malcolm, et al.
Infection Control and Hospital Epidemiology|December 1, 1995
Contaminated foods in healthcare facilitiesS Brooks, S Malcolm, P Lamont, et al.
Pageof 28