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W Wuyts

Showing results (21-30 of 51) with videos related to

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European Journal of Radiology|December 4, 2001
Hereditary multiple exostoses: from genetics to clinical syndrome and complicationsF M Vanhoenacker, W Van Hul, W Wuyts, et al.
European Journal of Cancer (Oxford, England : 1990)|April 28, 2004
Molecular analysis of the putative tumour-suppressor gene EXTL1 in neuroblastoma patients and cell linesD Mathysen, N Van Roy, W Van Hul, et al.
Pulmonology|September 14, 2024
"Alveolar stem cell exhaustion, fibrosis and bronchiolar proliferation" related entities. A narrative reviewM Chilosi, S Piciucchi, C Ravaglia, et al.
Human Molecular Genetics|April 18, 2000
Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagnaW Wuyts, W Reardon, S Preis, et al.
Clinical Genetics|September 5, 2001
Lack of mutations in the RANK gene in Spanish patients with Paget disease of boneM Marco-Mingot, J L San-Millán, W Wuyts, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|June 27, 2022
Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresiaJ Mortier, J van den Ende, F Declau, et al.
American Journal of Human Genetics|August 1, 1997
Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21W Van Hul, J Bollerslev, J Gram, et al.
Acta Clinica Belgica|June 18, 2015
The inner and outer of our thorax: silicone breast implants and pulmonary alveolar proteinosisH De Backer, K Darquennes, C Dooms, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplicationM Gentile, W Wuyts, S Grittani, et al.
British Journal of Cancer|July 20, 2001
A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosisC Y Xiao, J Wang, S Z Zhang, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
European Journal of Radiology|December 4, 2001
Hereditary multiple exostoses: from genetics to clinical syndrome and complicationsF M Vanhoenacker, W Van Hul, W Wuyts, et al.
European Journal of Cancer (Oxford, England : 1990)|April 28, 2004
Molecular analysis of the putative tumour-suppressor gene EXTL1 in neuroblastoma patients and cell linesD Mathysen, N Van Roy, W Van Hul, et al.
Pulmonology|September 14, 2024
"Alveolar stem cell exhaustion, fibrosis and bronchiolar proliferation" related entities. A narrative reviewM Chilosi, S Piciucchi, C Ravaglia, et al.
Human Molecular Genetics|April 18, 2000
Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagnaW Wuyts, W Reardon, S Preis, et al.
Clinical Genetics|September 5, 2001
Lack of mutations in the RANK gene in Spanish patients with Paget disease of boneM Marco-Mingot, J L San-Millán, W Wuyts, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|June 27, 2022
Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresiaJ Mortier, J van den Ende, F Declau, et al.
American Journal of Human Genetics|August 1, 1997
Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21W Van Hul, J Bollerslev, J Gram, et al.
Acta Clinica Belgica|June 18, 2015
The inner and outer of our thorax: silicone breast implants and pulmonary alveolar proteinosisH De Backer, K Darquennes, C Dooms, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplicationM Gentile, W Wuyts, S Grittani, et al.
British Journal of Cancer|July 20, 2001
A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosisC Y Xiao, J Wang, S Z Zhang, et al.
Pageof 6