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S Mundlos

Showing results (41-50 of 94) with videos related to

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Genetic Counseling (Geneva, Switzerland)|June 6, 2015
Neuroimaging and clinical characterization of Sotos syndromeS Türkmen, S Şahin, N Koçer, et al.
Development (Cambridge, England)|February 15, 2001
Sonic hedgehog is a survival factor for hypaxial muscles during mouse developmentM Krüger, D Mennerich, S Fees, et al.
Human Molecular Genetics|October 1, 1994
Alternative splicing as the result of a type II procollagen gene (COL2A1) mutation in a patient with Kniest dysplasiaA Winterpacht, U Schwarze, S Mundlos, et al.
Human Mutation|January 1, 1994
Autosomal dominant spondylarthropathy due to a type II procollagen gene (COL2A1) point mutationA Winterpacht, M Hilbert, U Schwarze, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 1, 1992
Detection of hepatitis B virus DNA in the liver of children with chronic hepatitis B by in situ hybridization and its relation to other viral markersS Wirth, A Hueter, I Blaha, et al.
Journal of Medical Genetics|January 8, 2008
A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndromeE Klopocki, C-E Ott, N Benatar, et al.
Nature Genetics|April 1, 1993
Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectA Winterpacht, M Hilbert, U Schwarze, et al.
The Journal of Biological Chemistry|January 27, 1995
A COL2A1 mutation in achondrogenesis type II results in the replacement of type II collagen by type I and III collagens in cartilageD Chan, W G Cole, C W Chow, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 1, 1997
Mouse clavicular development: analysis of wild-type and cleidocranial dysplasia mutant miceL F Huang, N Fukai, P B Selby, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|September 17, 2017
A novel COL1A2 C-propeptide cleavage site mutation causing high bone mass osteogenesis imperfecta with a regional distribution patternT Rolvien, U Kornak, J Stürznickel, et al.
Pageof 10

Showing results (41-50 of 94) with videos related to

Sort By:
Pageof 10
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
Neuroimaging and clinical characterization of Sotos syndromeS Türkmen, S Şahin, N Koçer, et al.
Development (Cambridge, England)|February 15, 2001
Sonic hedgehog is a survival factor for hypaxial muscles during mouse developmentM Krüger, D Mennerich, S Fees, et al.
Human Molecular Genetics|October 1, 1994
Alternative splicing as the result of a type II procollagen gene (COL2A1) mutation in a patient with Kniest dysplasiaA Winterpacht, U Schwarze, S Mundlos, et al.
Human Mutation|January 1, 1994
Autosomal dominant spondylarthropathy due to a type II procollagen gene (COL2A1) point mutationA Winterpacht, M Hilbert, U Schwarze, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 1, 1992
Detection of hepatitis B virus DNA in the liver of children with chronic hepatitis B by in situ hybridization and its relation to other viral markersS Wirth, A Hueter, I Blaha, et al.
Journal of Medical Genetics|January 8, 2008
A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndromeE Klopocki, C-E Ott, N Benatar, et al.
Nature Genetics|April 1, 1993
Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectA Winterpacht, M Hilbert, U Schwarze, et al.
The Journal of Biological Chemistry|January 27, 1995
A COL2A1 mutation in achondrogenesis type II results in the replacement of type II collagen by type I and III collagens in cartilageD Chan, W G Cole, C W Chow, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 1, 1997
Mouse clavicular development: analysis of wild-type and cleidocranial dysplasia mutant miceL F Huang, N Fukai, P B Selby, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|September 17, 2017
A novel COL1A2 C-propeptide cleavage site mutation causing high bone mass osteogenesis imperfecta with a regional distribution patternT Rolvien, U Kornak, J Stürznickel, et al.
Pageof 10