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C Hamel

Showing results (221-230 of 291) with videos related to

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Case Reports in Genetics|February 25, 2020
A Tanzanian Boy with Molecularly Confirmed X-Linked AdrenoleukodystrophyM C J Dekker, A M Sadiq, R Mc Larty, et al.
Phlebologie|April 1, 1992
[Return to work after surgical treatment of varicosities of the lower limb]C Vaislic, P Clerc, G Cloitre, et al.
Nature Genetics|January 1, 1996
A mutation in the gene encoding the alpha 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2)Y Muragaki, E C Mariman, S E van Beersum, et al.
Human Reproduction (Oxford, England)|March 25, 2022
Predicting the likelihood of successful medical treatment of early pregnancy loss: development and internal validation of a clinical prediction modelC C Hamel, P Vart, F P H A Vandenbussche, et al.
Clinical Genetics|September 8, 2011
Audiological findings in 100 USH2 patientsC Abadie, C Blanchet, D Baux, et al.
American Journal of Medical Genetics|July 12, 1996
A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28B C Hamel, H Kremer, E Wesby-van Swaay, et al.
The British Journal of Dermatology|July 2, 2011
Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assayM Refke, S M Pasternack, B Fiebig, et al.
Human Genetics|November 1, 1996
Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhoodH Kremer, B C Hamel, B van den Helm, et al.
British Journal of Cancer|December 10, 1999
Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2T J Hulsebos, N T Oskam, E H Bijleveld, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 25, 1998
Altered regulation of platelet-derived growth factor receptor-alpha gene-transcription in vitro by spina bifida-associated mutant Pax1 proteinsP H Joosten, F A Hol, S E van Beersum, et al.
Pageof 30

Showing results (221-230 of 291) with videos related to

Sort By:
Pageof 30
Case Reports in Genetics|February 25, 2020
A Tanzanian Boy with Molecularly Confirmed X-Linked AdrenoleukodystrophyM C J Dekker, A M Sadiq, R Mc Larty, et al.
Phlebologie|April 1, 1992
[Return to work after surgical treatment of varicosities of the lower limb]C Vaislic, P Clerc, G Cloitre, et al.
Nature Genetics|January 1, 1996
A mutation in the gene encoding the alpha 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2)Y Muragaki, E C Mariman, S E van Beersum, et al.
Human Reproduction (Oxford, England)|March 25, 2022
Predicting the likelihood of successful medical treatment of early pregnancy loss: development and internal validation of a clinical prediction modelC C Hamel, P Vart, F P H A Vandenbussche, et al.
Clinical Genetics|September 8, 2011
Audiological findings in 100 USH2 patientsC Abadie, C Blanchet, D Baux, et al.
American Journal of Medical Genetics|July 12, 1996
A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28B C Hamel, H Kremer, E Wesby-van Swaay, et al.
The British Journal of Dermatology|July 2, 2011
Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assayM Refke, S M Pasternack, B Fiebig, et al.
Human Genetics|November 1, 1996
Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhoodH Kremer, B C Hamel, B van den Helm, et al.
British Journal of Cancer|December 10, 1999
Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2T J Hulsebos, N T Oskam, E H Bijleveld, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 25, 1998
Altered regulation of platelet-derived growth factor receptor-alpha gene-transcription in vitro by spina bifida-associated mutant Pax1 proteinsP H Joosten, F A Hol, S E van Beersum, et al.
Pageof 30