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S Mundlos

Showing results (71-80 of 94) with videos related to

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Journal of Medical Genetics|April 5, 2005
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)K W Kjaer, L Hansen, G C Schwabe, 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|March 30, 2018
Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2S Butscheidt, A Delsmann, T Rolvien, et al.
Osteoarthritis and Cartilage|January 21, 2020
Skeletal deterioration in COL2A1-related spondyloepiphyseal dysplasia occurs prior to osteoarthritisT Rolvien, T A Yorgan, U Kornak, et al.
Journal of Medical Genetics|February 27, 2004
Acropectorovertebral dysgenesis (F syndrome) maps to chromosome 2q36H Thiele, C McCann, S van't Padje, et al.
American Journal of Human Genetics|June 23, 1998
Acromesomelic dysplasia Maroteaux type maps to human chromosome 9S G Kant, A Polinkovsky, S Mundlos, et al.
American Journal of Human Genetics|September 14, 2000
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type BG C Schwabe, S Tinschert, C Buschow, et al.
Heart (British Cardiac Society)|February 16, 2005
Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndromeW Heinritz, A Moschik, A Kujat, et al.
American Journal of Human Genetics|April 28, 2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tardaG E Tiller, V L Hannig, D Dozier, et al.
Journal of Biomechanics|May 19, 2009
Biaxial cell stimulation: A mechanical validationF H Bieler, C E Ott, M S Thompson, et al.
Journal of Medical Genetics|June 28, 2005
Breakpoints around the HOXD cluster result in various limb malformationsB Dlugaszewska, A Silahtaroglu, C Menzel, et al.
Pageof 10

Showing results (71-80 of 94) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|April 5, 2005
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)K W Kjaer, L Hansen, G C Schwabe, 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|March 30, 2018
Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2S Butscheidt, A Delsmann, T Rolvien, et al.
Osteoarthritis and Cartilage|January 21, 2020
Skeletal deterioration in COL2A1-related spondyloepiphyseal dysplasia occurs prior to osteoarthritisT Rolvien, T A Yorgan, U Kornak, et al.
Journal of Medical Genetics|February 27, 2004
Acropectorovertebral dysgenesis (F syndrome) maps to chromosome 2q36H Thiele, C McCann, S van't Padje, et al.
American Journal of Human Genetics|June 23, 1998
Acromesomelic dysplasia Maroteaux type maps to human chromosome 9S G Kant, A Polinkovsky, S Mundlos, et al.
American Journal of Human Genetics|September 14, 2000
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type BG C Schwabe, S Tinschert, C Buschow, et al.
Heart (British Cardiac Society)|February 16, 2005
Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndromeW Heinritz, A Moschik, A Kujat, et al.
American Journal of Human Genetics|April 28, 2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tardaG E Tiller, V L Hannig, D Dozier, et al.
Journal of Biomechanics|May 19, 2009
Biaxial cell stimulation: A mechanical validationF H Bieler, C E Ott, M S Thompson, et al.
Journal of Medical Genetics|June 28, 2005
Breakpoints around the HOXD cluster result in various limb malformationsB Dlugaszewska, A Silahtaroglu, C Menzel, et al.
Pageof 10