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M G BUTLER

Showing results (11-20 of 165) with videos related to

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Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|December 1, 1995
Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseasesR S Larson, M G Butler
American Journal of Medical Genetics|December 1, 1988
Do some patients with fragile X syndrome have precocious puberty?M G Butler, J L Najjar
American Journal of Physical Anthropology|December 1, 1987
Craniofacial variation and growth in the Prader-Labhart-Willi syndromeF J Meaney, M G Butler
Journal of Clinical Epigenetics|January 24, 2017
Examination of Global Methylation and Targeted Imprinted Genes in Prader-Willi SyndromeA M Manzardo, M G Butler
The International Journal of Pediatric Nephrology|October 1, 1987
Renal and urinary tract abnormalities associated with chromosome aberrationsA Y Barakat, M G Butler
American Journal of Medical Genetics|February 1, 1987
An anthropometric study of 38 individuals with Prader-Labhart-Willi syndromeM G Butler, F J Meaney
Pediatrics|October 1, 1991
Standards for selected anthropometric measurements in Prader-Willi syndromeM G Butler, F J Meaney
Journal of Intellectual Disability Research : JIDR|April 1, 1993
Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndromeM G Butler, D N Singh
American Journal of Medical Genetics|December 1, 1987
Sister chromatid exchange analysis in the Prader-Labhart-Willi syndromeM G Butler, B B Jenkins
Clinical Genetics|February 1, 1987
Robinow syndrome: report of two patients and review of literatureM G Butler, W B Wadlington
Pageof 17

Showing results (11-20 of 165) with videos related to

Sort By:
Pageof 17
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|December 1, 1995
Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseasesR S Larson, M G Butler
American Journal of Medical Genetics|December 1, 1988
Do some patients with fragile X syndrome have precocious puberty?M G Butler, J L Najjar
American Journal of Physical Anthropology|December 1, 1987
Craniofacial variation and growth in the Prader-Labhart-Willi syndromeF J Meaney, M G Butler
Journal of Clinical Epigenetics|January 24, 2017
Examination of Global Methylation and Targeted Imprinted Genes in Prader-Willi SyndromeA M Manzardo, M G Butler
The International Journal of Pediatric Nephrology|October 1, 1987
Renal and urinary tract abnormalities associated with chromosome aberrationsA Y Barakat, M G Butler
American Journal of Medical Genetics|February 1, 1987
An anthropometric study of 38 individuals with Prader-Labhart-Willi syndromeM G Butler, F J Meaney
Pediatrics|October 1, 1991
Standards for selected anthropometric measurements in Prader-Willi syndromeM G Butler, F J Meaney
Journal of Intellectual Disability Research : JIDR|April 1, 1993
Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndromeM G Butler, D N Singh
American Journal of Medical Genetics|December 1, 1987
Sister chromatid exchange analysis in the Prader-Labhart-Willi syndromeM G Butler, B B Jenkins
Clinical Genetics|February 1, 1987
Robinow syndrome: report of two patients and review of literatureM G Butler, W B Wadlington
Pageof 17