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P Coucke

Showing results (141-150 of 157) with videos related to

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American Journal of Medical Genetics|July 23, 1998
Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31J H Greinwald, S Wayne, A H Chen, et al.
Human Reproduction (Oxford, England)|February 20, 2021
Comparative analysis of mouse and human preimplantation development following POU5F1 CRISPR/Cas9 targeting reveals interspecies differencesP Stamatiadis, A Boel, G Cosemans, et al.
Genome Research|October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6K Fukushima, A Ramesh, C R Srisailapathy, et al.
Human Molecular Genetics|March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26M S Tomek, M R Brown, S R Mani, et al.
Journal of Medical Genetics|August 3, 2001
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairmentL Van Laer, P Coucke, R F Mueller, et al.
Journal of Medical Genetics|September 13, 2005
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 geneK P Hoornaert, C Dewinter, I Vereecke, et al.
Scientific Reports|February 16, 2016
Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and SkinC Gistelinck, R Gioia, A Gagliardi, et al.
Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|May 4, 1999
The value of pretreatment cell kinetic parameters as predictors for radiotherapy outcome in head and neck cancer: a multicenter analysisA C Begg, K Haustermans, A A Hart, et al.
Pageof 16

Showing results (141-150 of 157) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics|July 23, 1998
Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31J H Greinwald, S Wayne, A H Chen, et al.
Human Reproduction (Oxford, England)|February 20, 2021
Comparative analysis of mouse and human preimplantation development following POU5F1 CRISPR/Cas9 targeting reveals interspecies differencesP Stamatiadis, A Boel, G Cosemans, et al.
Genome Research|October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6K Fukushima, A Ramesh, C R Srisailapathy, et al.
Human Molecular Genetics|March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26M S Tomek, M R Brown, S R Mani, et al.
Journal of Medical Genetics|August 3, 2001
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairmentL Van Laer, P Coucke, R F Mueller, et al.
Journal of Medical Genetics|September 13, 2005
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 geneK P Hoornaert, C Dewinter, I Vereecke, et al.
Scientific Reports|February 16, 2016
Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and SkinC Gistelinck, R Gioia, A Gagliardi, et al.
Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|May 4, 1999
The value of pretreatment cell kinetic parameters as predictors for radiotherapy outcome in head and neck cancer: a multicenter analysisA C Begg, K Haustermans, A A Hart, et al.
Pageof 16