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H Leonard

Showing results (221-230 of 236) with videos related to

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BMC Developmental Biology|May 30, 2015
The Aurora A-HP1γ pathway regulates gene expression and mitosis in cells from the sperm lineagePhoebe H Leonard, Adrienne Grzenda, Angela Mathison, et al.
Epilepsy Research|January 18, 2024
Adapting a measure of gross motor skills for individuals with CDKL5 deficiency disorder: A psychometric studyJ M Saldaris, P Jacoby, E D Marsh, et al.
Human Molecular Genetics|April 18, 2000
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and locationJ P Cheadle, H Gill, N Fleming, et al.
Journal of Orthopaedic Trauma|April 4, 2023
Functional Outcomes of Primary Arthrodesis (PA) Versus Open Reduction and Internal Fixation (ORIF) in the Treatment of Lisfranc InjuriesArun Aneja, Zsombor T Gal, Ashley N Dawson, et al.
Journal of Medical Genetics|May 15, 2003
Mutation analysis in the MECP2 gene and genetic counselling for Rett syndromeH Gill, J P Cheadle, J Maynard, et al.
British Journal of Cancer|March 25, 2000
Mutation analysis of P73 and TP53 in Merkel cell carcinomaM Van Gele, M Kaghad, J H Leonard, et al.
Neurology|July 13, 2006
Early progressive encephalopathy in boys and MECP2 mutationsP Kankirawatana, H Leonard, C Ellaway, et al.
Genes, Chromosomes & Cancer|August 26, 1998
Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomasM Van Gele, N Van Roy, S G Ronan, et al.
Molecular Psychiatry|June 10, 2015
Autism risk associated with parental age and with increasing difference in age between the parentsS Sandin, D Schendel, P Magnusson, et al.
Brain & Development|May 30, 2001
Guidelines for reporting clinical features in cases with MECP2 mutationsA M Kerr, Y Nomura, D Armstrong, et al.
Pageof 24

Showing results (221-230 of 236) with videos related to

Sort By:
Pageof 24
BMC Developmental Biology|May 30, 2015
The Aurora A-HP1γ pathway regulates gene expression and mitosis in cells from the sperm lineagePhoebe H Leonard, Adrienne Grzenda, Angela Mathison, et al.
Epilepsy Research|January 18, 2024
Adapting a measure of gross motor skills for individuals with CDKL5 deficiency disorder: A psychometric studyJ M Saldaris, P Jacoby, E D Marsh, et al.
Human Molecular Genetics|April 18, 2000
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and locationJ P Cheadle, H Gill, N Fleming, et al.
Journal of Orthopaedic Trauma|April 4, 2023
Functional Outcomes of Primary Arthrodesis (PA) Versus Open Reduction and Internal Fixation (ORIF) in the Treatment of Lisfranc InjuriesArun Aneja, Zsombor T Gal, Ashley N Dawson, et al.
Journal of Medical Genetics|May 15, 2003
Mutation analysis in the MECP2 gene and genetic counselling for Rett syndromeH Gill, J P Cheadle, J Maynard, et al.
British Journal of Cancer|March 25, 2000
Mutation analysis of P73 and TP53 in Merkel cell carcinomaM Van Gele, M Kaghad, J H Leonard, et al.
Neurology|July 13, 2006
Early progressive encephalopathy in boys and MECP2 mutationsP Kankirawatana, H Leonard, C Ellaway, et al.
Genes, Chromosomes & Cancer|August 26, 1998
Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomasM Van Gele, N Van Roy, S G Ronan, et al.
Molecular Psychiatry|June 10, 2015
Autism risk associated with parental age and with increasing difference in age between the parentsS Sandin, D Schendel, P Magnusson, et al.
Brain & Development|May 30, 2001
Guidelines for reporting clinical features in cases with MECP2 mutationsA M Kerr, Y Nomura, D Armstrong, et al.
Pageof 24