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Showing results (71-80 of 89) with videos related to

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Genomics|May 18, 1999
A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36H C Heus, A Hing, M J van Baren, et al.
Neuroscience Letters|October 26, 1999
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian casesV Bonifati, M Joosse, D J Nicholl, et al.
American Journal of Human Genetics|July 20, 2001
Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36C M van Duijn, M C Dekker, V Bonifati, et al.
Genomics|September 16, 1999
Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21S Froelich, H Houlden, P Rizzu, et al.
Neurology|February 12, 2004
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson diseaseK Hedrich, A Djarmati, N Schäfer, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7V Bonifati, M C J Dekker, N Vanacore, et al.
Nature Genetics|February 14, 1998
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyB Brais, J P Bouchard, Y G Xie, et al.
Neurobiology of Aging|September 19, 2016
Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's diseaseS J Lubbe, V Escott-Price, A Brice, et al.
BMC Medical Genetics|July 20, 2015
Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcomeW Kelmemi, M E Teeuw, Z Bochdanovits, et al.
Human Molecular Genetics|August 11, 1999
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndromeM Kalff-Suske, A Wild, J Topp, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Genomics|May 18, 1999
A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36H C Heus, A Hing, M J van Baren, et al.
Neuroscience Letters|October 26, 1999
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian casesV Bonifati, M Joosse, D J Nicholl, et al.
American Journal of Human Genetics|July 20, 2001
Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36C M van Duijn, M C Dekker, V Bonifati, et al.
Genomics|September 16, 1999
Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21S Froelich, H Houlden, P Rizzu, et al.
Neurology|February 12, 2004
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson diseaseK Hedrich, A Djarmati, N Schäfer, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7V Bonifati, M C J Dekker, N Vanacore, et al.
Nature Genetics|February 14, 1998
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyB Brais, J P Bouchard, Y G Xie, et al.
Neurobiology of Aging|September 19, 2016
Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's diseaseS J Lubbe, V Escott-Price, A Brice, et al.
BMC Medical Genetics|July 20, 2015
Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcomeW Kelmemi, M E Teeuw, Z Bochdanovits, et al.
Human Molecular Genetics|August 11, 1999
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndromeM Kalff-Suske, A Wild, J Topp, et al.
Pageof 9