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J Meijers

Showing results (51-60 of 126) with videos related to

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American Journal of Medical Genetics|June 5, 1995
Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis)P E Taschner, N de Vos, J G Post, et al.
American Journal of Medical Genetics|August 3, 2001
Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndromeC H Wouters, H J Meijers-Heijboer, B J Eussen, et al.
Melanoma Research|February 6, 2025
Genetic concordance in melanoma: insights from primary tumors and their matched distant metastasesThamila Kerkour, Ruud W J Meijers, Loes M Hollestein, et al.
European Journal of Endocrinology|October 29, 2019
Leptin receptor deficiency: a systematic literature review and prevalence estimation based on population geneticsLotte Kleinendorst, Ozair Abawi, Hetty J van der Kamp, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Men at risk of being a mutation carrier for hereditary breast/ovarian cancer: an exploration of attitudes and psychological functioning during genetic testingL Lodder, P G Frets, R W Trijsburg, et al.
Molecular Cytogenetics|June 26, 2019
One-fits-all pretreatment protocol facilitating Fluorescence In Situ Hybridization on formalin-fixed paraffin-embedded, fresh frozen and cytological slidesShivanand O Richardson, Manon M H Huibers, Roel A de Weger, et al.
Journal of Medical Genetics|December 1, 1992
Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndromeE J Meijers-Heijboer, L A Sandkuijl, H G Brunner, et al.
Journal of Medical Genetics|June 19, 2002
What do women really want to know? Motives for attending familial breast cancer clinicsC J Van Asperen, S Van Dijk, M W Zoeteweij, et al.
British Journal of Cancer|December 21, 2019
No evidence for increased prevalence of colorectal carcinoma in 399 Dutch patients with Birt-Hogg-Dubé syndromeIrma van de Beek, Iris E Glykofridis, Rob M F Wolthuis, et al.
European Journal of Human Genetics : EJHG|September 11, 2014
Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndromeGea Beunders, Sonja A de Munnik, Nathalie Van der Aa, et al.
Pageof 13

Showing results (51-60 of 126) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|June 5, 1995
Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis)P E Taschner, N de Vos, J G Post, et al.
American Journal of Medical Genetics|August 3, 2001
Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndromeC H Wouters, H J Meijers-Heijboer, B J Eussen, et al.
Melanoma Research|February 6, 2025
Genetic concordance in melanoma: insights from primary tumors and their matched distant metastasesThamila Kerkour, Ruud W J Meijers, Loes M Hollestein, et al.
European Journal of Endocrinology|October 29, 2019
Leptin receptor deficiency: a systematic literature review and prevalence estimation based on population geneticsLotte Kleinendorst, Ozair Abawi, Hetty J van der Kamp, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Men at risk of being a mutation carrier for hereditary breast/ovarian cancer: an exploration of attitudes and psychological functioning during genetic testingL Lodder, P G Frets, R W Trijsburg, et al.
Molecular Cytogenetics|June 26, 2019
One-fits-all pretreatment protocol facilitating Fluorescence In Situ Hybridization on formalin-fixed paraffin-embedded, fresh frozen and cytological slidesShivanand O Richardson, Manon M H Huibers, Roel A de Weger, et al.
Journal of Medical Genetics|December 1, 1992
Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndromeE J Meijers-Heijboer, L A Sandkuijl, H G Brunner, et al.
Journal of Medical Genetics|June 19, 2002
What do women really want to know? Motives for attending familial breast cancer clinicsC J Van Asperen, S Van Dijk, M W Zoeteweij, et al.
British Journal of Cancer|December 21, 2019
No evidence for increased prevalence of colorectal carcinoma in 399 Dutch patients with Birt-Hogg-Dubé syndromeIrma van de Beek, Iris E Glykofridis, Rob M F Wolthuis, et al.
European Journal of Human Genetics : EJHG|September 11, 2014
Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndromeGea Beunders, Sonja A de Munnik, Nathalie Van der Aa, et al.
Pageof 13