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Showing results (11-20 of 17) with videos related to

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Nature Genetics|March 31, 2000
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossificationA O Wilkie, Z Tang, N Elanko, et al.
Nature Genetics|January 4, 2001
Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defectsL A Mavrogiannis, I Antonopoulou, A Baxová, et al.
American Journal of Human Genetics|March 11, 2000
Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndromeR L Glaser, W Jiang, S A Boyadjiev, et al.
American Journal of Human Genetics|February 11, 1999
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndromeM Oldridge, E H Zackai, D M McDonald-McGinn, et al.
American Journal of Human Genetics|October 30, 1998
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1D Johnson, S W Horsley, D M Moloney, et al.
Clinical Genetics|April 29, 2005
Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephalyF S Jehee, D Johnson, L G Alonso, et al.
American Journal of Human Genetics|March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeM Muenke, K W Gripp, D M McDonald-McGinn, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Nature Genetics|March 31, 2000
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossificationA O Wilkie, Z Tang, N Elanko, et al.
Nature Genetics|January 4, 2001
Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defectsL A Mavrogiannis, I Antonopoulou, A Baxová, et al.
American Journal of Human Genetics|March 11, 2000
Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndromeR L Glaser, W Jiang, S A Boyadjiev, et al.
American Journal of Human Genetics|February 11, 1999
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndromeM Oldridge, E H Zackai, D M McDonald-McGinn, et al.
American Journal of Human Genetics|October 30, 1998
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1D Johnson, S W Horsley, D M Moloney, et al.
Clinical Genetics|April 29, 2005
Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephalyF S Jehee, D Johnson, L G Alonso, et al.
American Journal of Human Genetics|March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeM Muenke, K W Gripp, D M McDonald-McGinn, et al.
Pageof 2