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David H Viskochil

Showing results (1-10 of 67) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 16, 2011
Disorders of the ras pathway: an introductionDavid H Viskochil
The Journal of Clinical Investigation|December 18, 2003
It takes two to tango: mast cell and Schwann cell interactions in neurofibromasDavid H Viskochil
American Journal of Medical Genetics|December 28, 2002
Status of the human malformation map: 2002John C Carey, David H Viskochil
American Journal of Medical Genetics. Part A|November 15, 2007
Status of the human malformation map: 2007John C Carey, David H Viskochil
American Journal of Medical Genetics. Part A|August 21, 2007
Neurofibromatosis type 1 is a genetic skeletal disorderDavid A Stevenson, David H Viskochil, John C Carey
Neurosurgical Focus|January 2, 2010
Neurofibromatosis Type 1 and tumorigenesis: molecular mechanisms and therapeutic implicationsOren N Gottfried, David H Viskochil, William T Couldwell
American Journal of Medical Genetics. Part A|June 24, 2004
Elevated catecholamine metabolites in patients with Costello syndromeKaren W Gripp, Hiroshi Kawame, David H Viskochil, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Speech-language characteristics of children with neurofibromatosis type 1Heather L Thompson, David H Viskochil, David A Stevenson, et al.
Neurosurgery|December 31, 2005
Molecular, genetic, and cellular pathogenesis of neurofibromas and surgical implicationsOren N Gottfried, David H Viskochil, Daniel W Fults, et al.
Journal of Pediatric Ophthalmology and Strabismus|May 1, 2014
Ophthalmologic features of Vici syndromeFrancis M Filloux, Robert O Hoffman, David H Viskochil, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 16, 2011
Disorders of the ras pathway: an introductionDavid H Viskochil
The Journal of Clinical Investigation|December 18, 2003
It takes two to tango: mast cell and Schwann cell interactions in neurofibromasDavid H Viskochil
American Journal of Medical Genetics|December 28, 2002
Status of the human malformation map: 2002John C Carey, David H Viskochil
American Journal of Medical Genetics. Part A|November 15, 2007
Status of the human malformation map: 2007John C Carey, David H Viskochil
American Journal of Medical Genetics. Part A|August 21, 2007
Neurofibromatosis type 1 is a genetic skeletal disorderDavid A Stevenson, David H Viskochil, John C Carey
Neurosurgical Focus|January 2, 2010
Neurofibromatosis Type 1 and tumorigenesis: molecular mechanisms and therapeutic implicationsOren N Gottfried, David H Viskochil, William T Couldwell
American Journal of Medical Genetics. Part A|June 24, 2004
Elevated catecholamine metabolites in patients with Costello syndromeKaren W Gripp, Hiroshi Kawame, David H Viskochil, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Speech-language characteristics of children with neurofibromatosis type 1Heather L Thompson, David H Viskochil, David A Stevenson, et al.
Neurosurgery|December 31, 2005
Molecular, genetic, and cellular pathogenesis of neurofibromas and surgical implicationsOren N Gottfried, David H Viskochil, Daniel W Fults, et al.
Journal of Pediatric Ophthalmology and Strabismus|May 1, 2014
Ophthalmologic features of Vici syndromeFrancis M Filloux, Robert O Hoffman, David H Viskochil, et al.
Pageof 7