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M K McCormack

Showing results (21-30 of 31) with videos related to

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The Journal of Pediatrics|September 1, 1976
Complex alpha-thalassemia-like syndrome: a cause of neonatal normoblastemiaM K McCormack, G R Geller, S Zak, et al.
Hemoglobin|January 1, 1986
Normal production of the mutant hemoglobin in heterozygotes for hemoglobin J-Paris and beta-thalassemiaM K McCormack, N Stone, F Desposito, et al.
The Journal of Pediatrics|June 1, 1976
Letter: A new kindred with hemoglobin Malmö (beta97 leads to Gln)M K McCormack, S J Zak, G R Geller, et al.
Cancer Genetics and Cytogenetics|October 15, 1988
Multiple chromosome aberrations in an infant with acute monoblastic leukemiaL E McMorrow, B H Greenbaum, S F Travis, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1975
Bis-(N-maleimidomethyl) ether: an antisickling reagentS J Zak, G R Geller, B Finkel, et al.
Pediatrics|December 1, 1975
A comparison of the physical and intellectual development of black children with and without sickle-cell traitM K McCormack, S Scarr-Salapatek, H Polesky, et al.
Human Biology|September 1, 1976
Growth patterns of children with sickle-cell diseaseM K McCormack, L Dicker, S H Katz, et al.
American Journal of Medical Genetics|July 17, 1995
Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20)A Lazzarini, E S Stenroos, T Lehner, et al.
Journal of Neurology|November 17, 2017
A new measure for end of life planning, preparation, and preferences in Huntington disease: HDQLIFE end of life planningNoelle E Carlozzi, E A Hahn, S A Frank, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|July 10, 2016
New measures to capture end of life concerns in Huntington disease: Meaning and Purpose and Concern with Death and Dying from HDQLIFE (a patient-reported outcomes measurement system)N E Carlozzi, N R Downing, M K McCormack, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
The Journal of Pediatrics|September 1, 1976
Complex alpha-thalassemia-like syndrome: a cause of neonatal normoblastemiaM K McCormack, G R Geller, S Zak, et al.
Hemoglobin|January 1, 1986
Normal production of the mutant hemoglobin in heterozygotes for hemoglobin J-Paris and beta-thalassemiaM K McCormack, N Stone, F Desposito, et al.
The Journal of Pediatrics|June 1, 1976
Letter: A new kindred with hemoglobin Malmö (beta97 leads to Gln)M K McCormack, S J Zak, G R Geller, et al.
Cancer Genetics and Cytogenetics|October 15, 1988
Multiple chromosome aberrations in an infant with acute monoblastic leukemiaL E McMorrow, B H Greenbaum, S F Travis, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1975
Bis-(N-maleimidomethyl) ether: an antisickling reagentS J Zak, G R Geller, B Finkel, et al.
Pediatrics|December 1, 1975
A comparison of the physical and intellectual development of black children with and without sickle-cell traitM K McCormack, S Scarr-Salapatek, H Polesky, et al.
Human Biology|September 1, 1976
Growth patterns of children with sickle-cell diseaseM K McCormack, L Dicker, S H Katz, et al.
American Journal of Medical Genetics|July 17, 1995
Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20)A Lazzarini, E S Stenroos, T Lehner, et al.
Journal of Neurology|November 17, 2017
A new measure for end of life planning, preparation, and preferences in Huntington disease: HDQLIFE end of life planningNoelle E Carlozzi, E A Hahn, S A Frank, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|July 10, 2016
New measures to capture end of life concerns in Huntington disease: Meaning and Purpose and Concern with Death and Dying from HDQLIFE (a patient-reported outcomes measurement system)N E Carlozzi, N R Downing, M K McCormack, et al.
Pageof 4