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G Brunner

Showing results (491-500 of 727) with videos related to

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Human Molecular Genetics|February 5, 1999
A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defectsY J de Kok, S J Bom, T M Brunt, et al.
American Journal of Human Genetics|August 16, 2006
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosisAnneke I den Hollander, Robert K Koenekoop, Suzanne Yzer, et al.
Journal of Medical Genetics|May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeJ van Reeuwijk, M Janssen, C van den Elzen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disordersRoos van der Donk, Sandra Jansen, Janneke H M Schuurs-Hoeijmakers, et al.
Magnetic Resonance in Medicine|September 21, 2022
Real-time trajectory guide tracking for intraoperative MRI-guided neurosurgeryMiles E Olsen, Ethan K Brodsky, Jonathan A Oler, et al.
Nature|March 6, 2009
Glycerol monolaurate prevents mucosal SIV transmissionQingsheng Li, Jacob D Estes, Patrick M Schlievert, et al.
Transplantation|September 7, 2001
Successful conversion from conventional immunosuppression to anti-CD154 monoclonal antibody costimulatory molecule blockade in rhesus renal allograft recipientsC S Cho, L C Burkly, J H Fechner, et al.
American Journal of Human Genetics|May 10, 2011
Chondrodysplasia and abnormal joint development associated with mutations in IMPAD1, encoding the Golgi-resident nucleotide phosphatase, gPAPPLisenka E L M Vissers, Ekkehart Lausch, Sheila Unger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2021
Diagnostic exome-based preconception carrier testing in consanguineous couples: results from the first 100 couples in clinical practiceSuzanne C E H Sallevelt, Alexander P A Stegmann, Bart de Koning, et al.
Nature Genetics|December 25, 2007
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2Uwe Kornak, Ellen Reynders, Aikaterini Dimopoulou, et al.
Pageof 73

Showing results (491-500 of 727) with videos related to

Sort By:
Pageof 73
Human Molecular Genetics|February 5, 1999
A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defectsY J de Kok, S J Bom, T M Brunt, et al.
American Journal of Human Genetics|August 16, 2006
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosisAnneke I den Hollander, Robert K Koenekoop, Suzanne Yzer, et al.
Journal of Medical Genetics|May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeJ van Reeuwijk, M Janssen, C van den Elzen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disordersRoos van der Donk, Sandra Jansen, Janneke H M Schuurs-Hoeijmakers, et al.
Magnetic Resonance in Medicine|September 21, 2022
Real-time trajectory guide tracking for intraoperative MRI-guided neurosurgeryMiles E Olsen, Ethan K Brodsky, Jonathan A Oler, et al.
Nature|March 6, 2009
Glycerol monolaurate prevents mucosal SIV transmissionQingsheng Li, Jacob D Estes, Patrick M Schlievert, et al.
Transplantation|September 7, 2001
Successful conversion from conventional immunosuppression to anti-CD154 monoclonal antibody costimulatory molecule blockade in rhesus renal allograft recipientsC S Cho, L C Burkly, J H Fechner, et al.
American Journal of Human Genetics|May 10, 2011
Chondrodysplasia and abnormal joint development associated with mutations in IMPAD1, encoding the Golgi-resident nucleotide phosphatase, gPAPPLisenka E L M Vissers, Ekkehart Lausch, Sheila Unger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2021
Diagnostic exome-based preconception carrier testing in consanguineous couples: results from the first 100 couples in clinical practiceSuzanne C E H Sallevelt, Alexander P A Stegmann, Bart de Koning, et al.
Nature Genetics|December 25, 2007
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2Uwe Kornak, Ellen Reynders, Aikaterini Dimopoulou, et al.
Pageof 73