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Showing results (21-30 of 27) with videos related to

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Journal of Medical Genetics|April 1, 1980
Amniocentesis in the West Midlands: report on 1000 birthsT Webb, J H Edwards, A H Cameron, et al.
The British Journal of Surgery|July 1, 1992
Role of congenital hypertrophy of the retinal pigment epithelium in the predictive diagnosis of familial adenomatous polyposisD G Morton, J Gibson, F Macdonald, et al.
Nature|January 26, 2000
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase geneG L Xu, T H Bestor, D Bourc'his, et al.
Lancet (London, England)|October 24, 1992
Germline APC mutation familial adenomatous polyposis in Indian familyY Wallis, F MacDonald, P M Rindl, 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.
Brain & Development|May 30, 2001
Guidelines for reporting clinical features in cases with MECP2 mutationsA M Kerr, Y Nomura, D Armstrong, et al.
Brain & Development|December 12, 2001
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved regionM Vacca, F Filippini, A Budillon, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Journal of Medical Genetics|April 1, 1980
Amniocentesis in the West Midlands: report on 1000 birthsT Webb, J H Edwards, A H Cameron, et al.
The British Journal of Surgery|July 1, 1992
Role of congenital hypertrophy of the retinal pigment epithelium in the predictive diagnosis of familial adenomatous polyposisD G Morton, J Gibson, F Macdonald, et al.
Nature|January 26, 2000
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase geneG L Xu, T H Bestor, D Bourc'his, et al.
Lancet (London, England)|October 24, 1992
Germline APC mutation familial adenomatous polyposis in Indian familyY Wallis, F MacDonald, P M Rindl, 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.
Brain & Development|May 30, 2001
Guidelines for reporting clinical features in cases with MECP2 mutationsA M Kerr, Y Nomura, D Armstrong, et al.
Brain & Development|December 12, 2001
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved regionM Vacca, F Filippini, A Budillon, et al.
Pageof 3