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American Journal of Medical Genetics
|
January 2, 1995
Proportions of spontaneous mutations in males and females with ornithine transcarbamylase deficiency
M Tuchman, I Matsuda, A Munnich, et al.
Human Genetics
|
February 1, 1992
Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndrome
J 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 disease
F 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 hermaphroditism
J 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 determination
A Pelham, M A O'Reilly, S Malcolm, et al.
Southern Medical Journal
|
November 1, 1978
Hepatic hemangioendotheliomas and hyperbilirubinemia
G 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 network
Sagheer 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 syndrome
K 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 phenotype
Philip J Mitchell, Elena Perez-Nadales, Denise S Malcolm, et al.
Infection Control and Hospital Epidemiology
|
December 1, 1995
Contaminated foods in healthcare facilities
S Brooks, S Malcolm, P Lamont, et al.
Page
of 28
Search research articles
Search
Showing results (111-120 of 271) with videos related to
Sort By:
Page
of 28
American Journal of Medical Genetics
|
January 2, 1995
Proportions of spontaneous mutations in males and females with ornithine transcarbamylase deficiency
M Tuchman, I Matsuda, A Munnich, et al.
Human Genetics
|
February 1, 1992
Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndrome
J 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 disease
F 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 hermaphroditism
J 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 determination
A Pelham, M A O'Reilly, S Malcolm, et al.
Southern Medical Journal
|
November 1, 1978
Hepatic hemangioendotheliomas and hyperbilirubinemia
G 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 network
Sagheer 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 syndrome
K 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 phenotype
Philip J Mitchell, Elena Perez-Nadales, Denise S Malcolm, et al.
Infection Control and Hospital Epidemiology
|
December 1, 1995
Contaminated foods in healthcare facilities
S Brooks, S Malcolm, P Lamont, et al.
Page
of 28