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G Brunner

Showing results (351-360 of 727) with videos related to

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Clinical Genetics|January 10, 2003
Very low incidence of microsatellite instability in rectal cancers from families at risk for HNPCCN Hoogerbrugge, R Willems, H J Van Krieken, et al.
Human Genetics|March 1, 1989
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)H G Brunner, R G Korneluk, M Coerwinkel-Driessen, et al.
American Journal of Medical Genetics. Part A|July 17, 2007
Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic mapIlse Feenstra, Lisenka E L M Vissers, Mirjam Orsel, et al.
BMC Women'S Health|May 10, 2012
DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-directAisha S Sie, Liesbeth Spruijt, Wendy A G van Zelst-Stams, et al.
Human Genetics|April 10, 2002
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephalyJeffrey E Ming, Michelle E Kaupas, Erich Roessler, et al.
European Journal of Human Genetics : EJHG|March 5, 2015
Syndromic X-linked intellectual disability segregating with a missense variant in RLIMElin Tønne, Rita Holdhus, Christine Stansberg, et al.
Plos Computational Biology|April 28, 2010
Accurate distinction of pathogenic from benign CNVs in mental retardationJayne Y Hehir-Kwa, Nienke Wieskamp, Caleb Webber, et al.
Nature Genetics|April 12, 2005
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndromeHans van Bokhoven, Jacopo Celli, Jeroen van Reeuwijk, et al.
British Journal of Cancer|November 23, 2006
Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instabilityC M Kets, J H J M van Krieken, K M Hebeda, et al.
Nature Genetics|August 10, 2000
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.
Pageof 73

Showing results (351-360 of 727) with videos related to

Sort By:
Pageof 73
Clinical Genetics|January 10, 2003
Very low incidence of microsatellite instability in rectal cancers from families at risk for HNPCCN Hoogerbrugge, R Willems, H J Van Krieken, et al.
Human Genetics|March 1, 1989
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)H G Brunner, R G Korneluk, M Coerwinkel-Driessen, et al.
American Journal of Medical Genetics. Part A|July 17, 2007
Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic mapIlse Feenstra, Lisenka E L M Vissers, Mirjam Orsel, et al.
BMC Women'S Health|May 10, 2012
DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-directAisha S Sie, Liesbeth Spruijt, Wendy A G van Zelst-Stams, et al.
Human Genetics|April 10, 2002
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephalyJeffrey E Ming, Michelle E Kaupas, Erich Roessler, et al.
European Journal of Human Genetics : EJHG|March 5, 2015
Syndromic X-linked intellectual disability segregating with a missense variant in RLIMElin Tønne, Rita Holdhus, Christine Stansberg, et al.
Plos Computational Biology|April 28, 2010
Accurate distinction of pathogenic from benign CNVs in mental retardationJayne Y Hehir-Kwa, Nienke Wieskamp, Caleb Webber, et al.
Nature Genetics|April 12, 2005
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndromeHans van Bokhoven, Jacopo Celli, Jeroen van Reeuwijk, et al.
British Journal of Cancer|November 23, 2006
Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instabilityC M Kets, J H J M van Krieken, K M Hebeda, et al.
Nature Genetics|August 10, 2000
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.
Pageof 73