Search research articles
Contact Us
Filters
Showing results (1-10 of 67) with videos related to
Page
of 7
Sort By:
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
April 16, 2011
Disorders of the ras pathway: an introduction
David H Viskochil
The Journal of Clinical Investigation
|
December 18, 2003
It takes two to tango: mast cell and Schwann cell interactions in neurofibromas
David H Viskochil
American Journal of Medical Genetics
|
December 28, 2002
Status of the human malformation map: 2002
John C Carey, David H Viskochil
American Journal of Medical Genetics. Part A
|
November 15, 2007
Status of the human malformation map: 2007
John C Carey, David H Viskochil
American Journal of Medical Genetics. Part A
|
August 21, 2007
Neurofibromatosis type 1 is a genetic skeletal disorder
David A Stevenson, David H Viskochil, John C Carey
Neurosurgical Focus
|
January 2, 2010
Neurofibromatosis Type 1 and tumorigenesis: molecular mechanisms and therapeutic implications
Oren 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 syndrome
Karen 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 1
Heather L Thompson, David H Viskochil, David A Stevenson, et al.
Neurosurgery
|
December 31, 2005
Molecular, genetic, and cellular pathogenesis of neurofibromas and surgical implications
Oren N Gottfried, David H Viskochil, Daniel W Fults, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
May 1, 2014
Ophthalmologic features of Vici syndrome
Francis M Filloux, Robert O Hoffman, David H Viskochil, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 67) with videos related to
Sort By:
Page
of 7
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
April 16, 2011
Disorders of the ras pathway: an introduction
David H Viskochil
The Journal of Clinical Investigation
|
December 18, 2003
It takes two to tango: mast cell and Schwann cell interactions in neurofibromas
David H Viskochil
American Journal of Medical Genetics
|
December 28, 2002
Status of the human malformation map: 2002
John C Carey, David H Viskochil
American Journal of Medical Genetics. Part A
|
November 15, 2007
Status of the human malformation map: 2007
John C Carey, David H Viskochil
American Journal of Medical Genetics. Part A
|
August 21, 2007
Neurofibromatosis type 1 is a genetic skeletal disorder
David A Stevenson, David H Viskochil, John C Carey
Neurosurgical Focus
|
January 2, 2010
Neurofibromatosis Type 1 and tumorigenesis: molecular mechanisms and therapeutic implications
Oren 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 syndrome
Karen 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 1
Heather L Thompson, David H Viskochil, David A Stevenson, et al.
Neurosurgery
|
December 31, 2005
Molecular, genetic, and cellular pathogenesis of neurofibromas and surgical implications
Oren N Gottfried, David H Viskochil, Daniel W Fults, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
May 1, 2014
Ophthalmologic features of Vici syndrome
Francis M Filloux, Robert O Hoffman, David H Viskochil, et al.
Page
of 7