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Showing results (51-60 of 54) with videos related to

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Journal of Medical Genetics|November 8, 2005
Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosaJ C Booij, R J Florijn, J B ten Brink, et al.
Acta Anaesthesiologica Scandinavica|January 21, 2012
Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndromeA V Vanlander, P G Jorens, J Smet, et al.
American Journal of Human Genetics|June 18, 2005
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndromeD Beysen, J Raes, B P Leroy, et al.
Human Molecular Genetics|July 27, 2001
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlationE De Baere, M J Dixon, K W Small, et al.
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Showing results (51-60 of 54) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 54 results.
Journal of Medical Genetics|November 8, 2005
Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosaJ C Booij, R J Florijn, J B ten Brink, et al.
Acta Anaesthesiologica Scandinavica|January 21, 2012
Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndromeA V Vanlander, P G Jorens, J Smet, et al.
American Journal of Human Genetics|June 18, 2005
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndromeD Beysen, J Raes, B P Leroy, et al.
Human Molecular Genetics|July 27, 2001
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlationE De Baere, M J Dixon, K W Small, et al.
Pageof 6