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M C Bakker

Showing results (1-10 of 8) with videos related to

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Nederlands Tijdschrift Voor Tandheelkunde|September 1, 1983
[3 years' clinical experience with impressions for crown and bridgework using a combination of reversible hydrocolloids and alginates]M C Bakker
Nederlands Tijdschrift Voor Tandheelkunde|June 1, 1977
[Oral myiasis]M C Bakker
Lancet (London, England)|January 20, 1996
Association of apolipoprotein E epsilon 4 allele with bulbar-onset motor neuron diseaseA al-Chalabi, Z E Enayat, M C Bakker, et al.
Clinical Genetics|February 27, 2013
Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegiaC Bettencourt, J L López-Sendón, J García-Caldentey, et al.
Plos One|November 27, 2013
Resequencing three candidate genes for major depressive disorder in a Dutch cohortEva C Verbeek, Marianna R Bevova, Zoltán Bochdanovits, et al.
Plos One|June 1, 2012
A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorderEva C Verbeek, Ingrid M C Bakker, Marianna R Bevova, et al.
Cerebellum (London, England)|January 17, 2015
Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1Conceição Bettencourt, Justo García de Yébenes, José Luis López-Sendón, et al.
Brain : a Journal of Neurology|March 14, 2013
Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathySietske H Kevelam, Marianna Bugiani, Gajja S Salomons, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Nederlands Tijdschrift Voor Tandheelkunde|September 1, 1983
[3 years' clinical experience with impressions for crown and bridgework using a combination of reversible hydrocolloids and alginates]M C Bakker
Nederlands Tijdschrift Voor Tandheelkunde|June 1, 1977
[Oral myiasis]M C Bakker
Lancet (London, England)|January 20, 1996
Association of apolipoprotein E epsilon 4 allele with bulbar-onset motor neuron diseaseA al-Chalabi, Z E Enayat, M C Bakker, et al.
Clinical Genetics|February 27, 2013
Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegiaC Bettencourt, J L López-Sendón, J García-Caldentey, et al.
Plos One|November 27, 2013
Resequencing three candidate genes for major depressive disorder in a Dutch cohortEva C Verbeek, Marianna R Bevova, Zoltán Bochdanovits, et al.
Plos One|June 1, 2012
A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorderEva C Verbeek, Ingrid M C Bakker, Marianna R Bevova, et al.
Cerebellum (London, England)|January 17, 2015
Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1Conceição Bettencourt, Justo García de Yébenes, José Luis López-Sendón, et al.
Brain : a Journal of Neurology|March 14, 2013
Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathySietske H Kevelam, Marianna Bugiani, Gajja S Salomons, et al.
Pageof 1