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S Malcolm

Showing results (171-180 of 271) with videos related to

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Human Genetics|July 1, 1988
Regional chromosomal localisation of APOA2 to 1q21-1q23H R Middleton-Price, J A van den Berghe, J Scott, et al.
Acta Neuropsychiatrica|March 24, 2023
Has maternal sensitivity been comprehensively investigated in sub-Saharan Africa? A narrative scoping reviewA Prag, K A Donald, E Weldon, et al.
Journal of Intellectual Disability Research : JIDR|February 15, 2023
Determining the neurocognitive profile of children with tuberous sclerosis complex within the Western Cape region of South AfricaN M Berghoff, J M Wilmshurst, T A Page, et al.
Biochemical Pharmacology|July 13, 2001
Agonist-induced functional desensitization of recombinant human 5-HT2 receptors expressed in CHO-K1 cellsR H Porter, C S Malcolm, N H Allen, et al.
Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.
Human Genetics|December 1, 1990
The major cystic fibrosis mutation in a British populationC J McMahon, S A Genet, H R Middleton-Price, et al.
Blood|May 1, 1988
Cellular and molecular studies on infant null acute lymphoblastic leukemiaF Katz, S Malcolm, B Gibbons, et al.
Genomics|February 1, 1989
Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markersH R Middleton-Price, A E Harding, J Berciano, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Three infants having null acute lymphoblastic leukemia with chromosome rearrangements at 11q23: no involvement of a heritable fragile site in this bandJ A van den Berghe, S Malcolm, F E Katz, et al.
Human Molecular Genetics|August 1, 1994
Angelman syndrome associated with a maternal 15q11-13 deletion of less than 200 kbJ L Buxton, C T Chan, H Gilbert, et al.
Pageof 28

Showing results (171-180 of 271) with videos related to

Sort By:
Pageof 28
Human Genetics|July 1, 1988
Regional chromosomal localisation of APOA2 to 1q21-1q23H R Middleton-Price, J A van den Berghe, J Scott, et al.
Acta Neuropsychiatrica|March 24, 2023
Has maternal sensitivity been comprehensively investigated in sub-Saharan Africa? A narrative scoping reviewA Prag, K A Donald, E Weldon, et al.
Journal of Intellectual Disability Research : JIDR|February 15, 2023
Determining the neurocognitive profile of children with tuberous sclerosis complex within the Western Cape region of South AfricaN M Berghoff, J M Wilmshurst, T A Page, et al.
Biochemical Pharmacology|July 13, 2001
Agonist-induced functional desensitization of recombinant human 5-HT2 receptors expressed in CHO-K1 cellsR H Porter, C S Malcolm, N H Allen, et al.
Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.
Human Genetics|December 1, 1990
The major cystic fibrosis mutation in a British populationC J McMahon, S A Genet, H R Middleton-Price, et al.
Blood|May 1, 1988
Cellular and molecular studies on infant null acute lymphoblastic leukemiaF Katz, S Malcolm, B Gibbons, et al.
Genomics|February 1, 1989
Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markersH R Middleton-Price, A E Harding, J Berciano, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Three infants having null acute lymphoblastic leukemia with chromosome rearrangements at 11q23: no involvement of a heritable fragile site in this bandJ A van den Berghe, S Malcolm, F E Katz, et al.
Human Molecular Genetics|August 1, 1994
Angelman syndrome associated with a maternal 15q11-13 deletion of less than 200 kbJ L Buxton, C T Chan, H Gilbert, et al.
Pageof 28