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P L Pearson

Showing results (201-210 of 211) with videos related to

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Human Molecular Genetics|February 9, 1999
Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16B J van de Sluis, M Breen, M Nanji, et al.
American Journal of Human Genetics|April 8, 2003
A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15qS C Bakker, E M van der Meulen, J K Buitelaar, et al.
Stroke|August 28, 2004
Genome-wide linkage in a large Dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13Y B W E M Roos, G Pals, P M Struycken, et al.
Journal of Medical Genetics|January 11, 2000
Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma onlyF J Hes, S McKee, M J Taphoorn, et al.
Human Mutation|January 11, 2000
Genetic variation in ICF syndrome: evidence for genetic heterogeneityC Wijmenga, R S Hansen, G Gimelli, et al.
American Journal of Human Genetics|August 27, 1998
Localization of the ICF syndrome to chromosome 20 by homozygosity mappingC Wijmenga, L P van den Heuvel, E Strengman, et al.
Human Genetics|September 1, 1997
Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64R J Sinke, V E Carlton, J A Juijn, et al.
Cytogenetic and Genome Research|November 25, 2006
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterationsA C V Krepischi-Santos, A M Vianna-Morgante, F S Jehee, et al.
American Journal of Medical Genetics|June 27, 1997
The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromesA M Zwamborn-Hanssen, J B Bijlsma, E F Hennekam, et al.
Clinical Genetics|July 31, 2007
Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplificationF J Hes, R B van der Luijt, A L W Janssen, et al.
Pageof 22

Showing results (201-210 of 211) with videos related to

Sort By:
Pageof 22
Human Molecular Genetics|February 9, 1999
Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16B J van de Sluis, M Breen, M Nanji, et al.
American Journal of Human Genetics|April 8, 2003
A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15qS C Bakker, E M van der Meulen, J K Buitelaar, et al.
Stroke|August 28, 2004
Genome-wide linkage in a large Dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13Y B W E M Roos, G Pals, P M Struycken, et al.
Journal of Medical Genetics|January 11, 2000
Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma onlyF J Hes, S McKee, M J Taphoorn, et al.
Human Mutation|January 11, 2000
Genetic variation in ICF syndrome: evidence for genetic heterogeneityC Wijmenga, R S Hansen, G Gimelli, et al.
American Journal of Human Genetics|August 27, 1998
Localization of the ICF syndrome to chromosome 20 by homozygosity mappingC Wijmenga, L P van den Heuvel, E Strengman, et al.
Human Genetics|September 1, 1997
Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64R J Sinke, V E Carlton, J A Juijn, et al.
Cytogenetic and Genome Research|November 25, 2006
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterationsA C V Krepischi-Santos, A M Vianna-Morgante, F S Jehee, et al.
American Journal of Medical Genetics|June 27, 1997
The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromesA M Zwamborn-Hanssen, J B Bijlsma, E F Hennekam, et al.
Clinical Genetics|July 31, 2007
Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplificationF J Hes, R B van der Luijt, A L W Janssen, et al.
Pageof 22