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M G BUTLER

Showing results (61-70 of 165) with videos related to

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Cancer Genetics and Cytogenetics|May 1, 1996
Lack of microsatellite instability in giant cell tumor of boneM Scheiner, L Hedges, H S Schwartz, et al.
Annals of Surgical Oncology|November 27, 1998
Telomerase activity in skeletal sarcomasG Aue, B Muralidhar, H S Schwartz, et al.
Journal of Medical Genetics|August 16, 2003
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPDD C Bittel, N Kibiryeva, Z Talebizadeh, et al.
Clinical Genetics|May 1, 1991
A 15-item checklist for screening mentally retarded males for the fragile X syndromeM G Butler, T Mangrum, R Gupta, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|January 1, 1997
Elevated plasma gamma-aminobutyric acid (GABA) levels in individuals with either Prader-Willi syndrome or Angelman syndromeM H Ebert, D E Schmidt, T Thompson, et al.
Clinical Genetics|December 8, 1998
Genetic variants of the human obesity (OB) gene in subjects with and without Prader-Willi syndrome: comparison with body mass index and weightM G Butler, L Hedges, C L Hovis, et al.
Pediatrics|June 1, 1992
Standards for selected anthropometric measurements in males with the fragile X syndromeM G Butler, A Brunschwig, L K Miller, et al.
Investigative Ophthalmology & Visual Science|March 11, 2000
Adenovirus keratitis: a role for interleukin-8J Chodosh, R A Astley, M G Butler, et al.
Child Nephrology and Urology|January 1, 1990
Focal sclerosing glomerulonephritis in a child with Laurence-Moon-Biedl syndromeA J Barakat, P Arianas, A D Glick, et al.
American Journal of Medical Genetics|October 16, 1996
A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13M G Butler, S L Christian, T Kubota, et al.
Pageof 17

Showing results (61-70 of 165) with videos related to

Sort By:
Pageof 17
Cancer Genetics and Cytogenetics|May 1, 1996
Lack of microsatellite instability in giant cell tumor of boneM Scheiner, L Hedges, H S Schwartz, et al.
Annals of Surgical Oncology|November 27, 1998
Telomerase activity in skeletal sarcomasG Aue, B Muralidhar, H S Schwartz, et al.
Journal of Medical Genetics|August 16, 2003
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPDD C Bittel, N Kibiryeva, Z Talebizadeh, et al.
Clinical Genetics|May 1, 1991
A 15-item checklist for screening mentally retarded males for the fragile X syndromeM G Butler, T Mangrum, R Gupta, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|January 1, 1997
Elevated plasma gamma-aminobutyric acid (GABA) levels in individuals with either Prader-Willi syndrome or Angelman syndromeM H Ebert, D E Schmidt, T Thompson, et al.
Clinical Genetics|December 8, 1998
Genetic variants of the human obesity (OB) gene in subjects with and without Prader-Willi syndrome: comparison with body mass index and weightM G Butler, L Hedges, C L Hovis, et al.
Pediatrics|June 1, 1992
Standards for selected anthropometric measurements in males with the fragile X syndromeM G Butler, A Brunschwig, L K Miller, et al.
Investigative Ophthalmology & Visual Science|March 11, 2000
Adenovirus keratitis: a role for interleukin-8J Chodosh, R A Astley, M G Butler, et al.
Child Nephrology and Urology|January 1, 1990
Focal sclerosing glomerulonephritis in a child with Laurence-Moon-Biedl syndromeA J Barakat, P Arianas, A D Glick, et al.
American Journal of Medical Genetics|October 16, 1996
A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13M G Butler, S L Christian, T Kubota, et al.
Pageof 17