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Showing results (11-20 of 16) with videos related to

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Genes, Chromosomes & Cancer|November 7, 2000
Inclusion of malignant fibrous histiocytoma in the tumour spectrum associated with hereditary non-polyposis colorectal cancerR Sijmons, R Hofstra, H Hollema, et al.
Journal of Medical Genetics|May 4, 2004
PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndromeI Matera, T Bachetti, F Puppo, et al.
American Journal of Human Genetics|June 12, 1999
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11R Wadey, J McKie, C Papapetrou, et al.
Nature Genetics|October 3, 1999
Familial endometrial cancer in female carriers of MSH6 germline mutationsJ Wijnen, W de Leeuw, H Vasen, et al.
Journal of Medical Genetics|May 23, 2001
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigreeA Wagner, Y Hendriks, E J Meijers-Heijboer, et al.
Journal of Medical Genetics|August 16, 2003
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wideB Wilcken, F Bamforth, Z Li, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Genes, Chromosomes & Cancer|November 7, 2000
Inclusion of malignant fibrous histiocytoma in the tumour spectrum associated with hereditary non-polyposis colorectal cancerR Sijmons, R Hofstra, H Hollema, et al.
Journal of Medical Genetics|May 4, 2004
PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndromeI Matera, T Bachetti, F Puppo, et al.
American Journal of Human Genetics|June 12, 1999
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11R Wadey, J McKie, C Papapetrou, et al.
Nature Genetics|October 3, 1999
Familial endometrial cancer in female carriers of MSH6 germline mutationsJ Wijnen, W de Leeuw, H Vasen, et al.
Journal of Medical Genetics|May 23, 2001
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigreeA Wagner, Y Hendriks, E J Meijers-Heijboer, et al.
Journal of Medical Genetics|August 16, 2003
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wideB Wilcken, F Bamforth, Z Li, et al.
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