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K Temple

Showing results (71-80 of 262) with videos related to

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Human Genetics|September 15, 2000
Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndromeC A Joyce, A Sharp, J M Walker, et al.
The Journal of Experimental Biology|February 21, 2002
Determining patterns of motor recruitment during locomotionJames M Wakeling, Motoshi Kaya, Genevieve K Temple, et al.
The Journal of Pediatrics|December 18, 2001
Skin spots and heart tumorsT D Reddy, D M Eccles, J Theaker, et al.
Genes, Chromosomes & Cancer|September 25, 2004
Application of combined immunofluorescence and fluorescence in situ hybridization on paraffin-embedded sections to characterize T-cell lymphoma with EBV-infected B-cell blastsGenevieve K Temple, Mark Sales, Neil Kernohan, et al.
BMJ Case Reports|July 7, 2011
Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14I K Temple, V Shrubb, M Lever, et al.
Journal of Mental Health (Abingdon, England)|December 2, 2020
Understanding practitioners' and young people's views of a risk calculator for future psychopathology and poor functioning in young people victimised during childhoodRachel M Latham, Rachel K Temple, Crystal Romeo, et al.
Clinical Genetics|January 23, 1999
Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitusR J Gardner, D O Robinson, L Lamont, et al.
American Journal of Medical Genetics|October 1, 1991
Genetic and clinical heterogeneity of Stickler syndromeG M Vintiner, I K Temple, H R Middleton-Price, et al.
Journal of Medical Genetics|July 1, 1989
Kyphomelic dysplasiaI K Temple, E M Thompson, C M Hall, et al.
American Journal of Medical Genetics|September 15, 1991
Dominantly inherited syndrome comprising partially absent eye muscles, hydrocephaly, skeletal abnormalities, and a distinctive facial phenotypeL S Chitty, R McCrimmon, I K Temple, et al.
Pageof 27

Showing results (71-80 of 262) with videos related to

Sort By:
Pageof 27
Human Genetics|September 15, 2000
Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndromeC A Joyce, A Sharp, J M Walker, et al.
The Journal of Experimental Biology|February 21, 2002
Determining patterns of motor recruitment during locomotionJames M Wakeling, Motoshi Kaya, Genevieve K Temple, et al.
The Journal of Pediatrics|December 18, 2001
Skin spots and heart tumorsT D Reddy, D M Eccles, J Theaker, et al.
Genes, Chromosomes & Cancer|September 25, 2004
Application of combined immunofluorescence and fluorescence in situ hybridization on paraffin-embedded sections to characterize T-cell lymphoma with EBV-infected B-cell blastsGenevieve K Temple, Mark Sales, Neil Kernohan, et al.
BMJ Case Reports|July 7, 2011
Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14I K Temple, V Shrubb, M Lever, et al.
Journal of Mental Health (Abingdon, England)|December 2, 2020
Understanding practitioners' and young people's views of a risk calculator for future psychopathology and poor functioning in young people victimised during childhoodRachel M Latham, Rachel K Temple, Crystal Romeo, et al.
Clinical Genetics|January 23, 1999
Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitusR J Gardner, D O Robinson, L Lamont, et al.
American Journal of Medical Genetics|October 1, 1991
Genetic and clinical heterogeneity of Stickler syndromeG M Vintiner, I K Temple, H R Middleton-Price, et al.
Journal of Medical Genetics|July 1, 1989
Kyphomelic dysplasiaI K Temple, E M Thompson, C M Hall, et al.
American Journal of Medical Genetics|September 15, 1991
Dominantly inherited syndrome comprising partially absent eye muscles, hydrocephaly, skeletal abnormalities, and a distinctive facial phenotypeL S Chitty, R McCrimmon, I K Temple, et al.
Pageof 27