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M P Lombardi

Showing results (1-10 of 14) with videos related to

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Molecular Human Reproduction|October 18, 2005
Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermiaG H Westerveld, S Repping, M P Lombardi, et al.
Frontiers in Genetics|July 21, 2022
Further Introduction of DNA Methylation (DNAm) Arrays in Regular DiagnosticsM M A M Mannens, M P Lombardi, M Alders, et al.
Cardiovascular Drugs and Therapy|October 24, 2001
CDNA arrays: the ups and downsC A Remme, M P Lombardi, M J van den Hoff, et al.
Molecular Human Reproduction|March 5, 2004
Heterogeneous nuclear ribonucleoprotein G-T (HNRNP G-T) mutations in men with impaired spermatogenesisG H Westerveld, J Gianotten, N J Leschot, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|January 1, 1996
Detection of cellular heterogeneity by DNA ploidy, 17 chromosome, and p53 gene in primary carcinoma and metastasis in a case of ovarian cancerA Calugi, P Eleuteri, D Cavallo, et al.
Human Genetics|August 1, 1997
Mutational and genetic origin of LDL receptor gene mutations detected in both Belgian and Dutch familial hypercholesterolemicsA V Peeters, L F Van Gaal, L du Plessis, et al.
Experientia|November 15, 1995
Antimitotic and antiviral activities of Kelletinin A in HTLV-1 infected MT2 cellsI Silvestri, L Albonici, M Ciotti, et al.
European Journal of Pediatrics|April 12, 2014
The value of DNA storage and pedigree analysis in rare diseases: a 17-year-old boy with X-linked lymphoproliferative disease (XLP) caused by a de novo SH2D1A mutationE Overwater, Y Smulders, M van der Burg, et al.
Genetic Testing|June 24, 2006
Molecular genetic testing for familial hypercholesterolemia in the Netherlands: a stepwise screening strategy enhances the mutation detection rateM P Lombardi, E J W Redeker, D H M van Gent, et al.
Human Reproduction (Oxford, England)|August 26, 2006
Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failureG H Westerveld, C M Korver, A M M van Pelt, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Molecular Human Reproduction|October 18, 2005
Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermiaG H Westerveld, S Repping, M P Lombardi, et al.
Frontiers in Genetics|July 21, 2022
Further Introduction of DNA Methylation (DNAm) Arrays in Regular DiagnosticsM M A M Mannens, M P Lombardi, M Alders, et al.
Cardiovascular Drugs and Therapy|October 24, 2001
CDNA arrays: the ups and downsC A Remme, M P Lombardi, M J van den Hoff, et al.
Molecular Human Reproduction|March 5, 2004
Heterogeneous nuclear ribonucleoprotein G-T (HNRNP G-T) mutations in men with impaired spermatogenesisG H Westerveld, J Gianotten, N J Leschot, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|January 1, 1996
Detection of cellular heterogeneity by DNA ploidy, 17 chromosome, and p53 gene in primary carcinoma and metastasis in a case of ovarian cancerA Calugi, P Eleuteri, D Cavallo, et al.
Human Genetics|August 1, 1997
Mutational and genetic origin of LDL receptor gene mutations detected in both Belgian and Dutch familial hypercholesterolemicsA V Peeters, L F Van Gaal, L du Plessis, et al.
Experientia|November 15, 1995
Antimitotic and antiviral activities of Kelletinin A in HTLV-1 infected MT2 cellsI Silvestri, L Albonici, M Ciotti, et al.
European Journal of Pediatrics|April 12, 2014
The value of DNA storage and pedigree analysis in rare diseases: a 17-year-old boy with X-linked lymphoproliferative disease (XLP) caused by a de novo SH2D1A mutationE Overwater, Y Smulders, M van der Burg, et al.
Genetic Testing|June 24, 2006
Molecular genetic testing for familial hypercholesterolemia in the Netherlands: a stepwise screening strategy enhances the mutation detection rateM P Lombardi, E J W Redeker, D H M van Gent, et al.
Human Reproduction (Oxford, England)|August 26, 2006
Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failureG H Westerveld, C M Korver, A M M van Pelt, et al.
Pageof 2