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Ultrastructural Pathology|May 1, 1988
Ultrastructural localization of antigens recognized by the monoclonal antibodies MB1, MB2, MT1, UCHL1, and TAL 1B5M G Butler, C Wells, A J d'ArdenneAmerican Journal of Medical Genetics|April 1, 1987
A 26-month-old child with Marden-Walker syndrome and pyloric stenosisD Gossage, J M Perrin, M G ButlerAmerican Journal of Medical Genetics|May 8, 2000
SPONASTRIME dysplasia: report of an 11-year-old boy and review of the literatureH A Cooper, J Crowe, M G ButlerJournal of Pediatric Ophthalmology and Strabismus|July 1, 1978
Cryptophthalmos with an orbital cyst and profound mental and motor retardationM G Butler, J D Eisen, J HenryCytogenetics and Cell Genetics|January 1, 1981
A unique Y/Y translocation in an infertile maleM G Butler, W G Sanger, M P WalzakAmerican Journal of Medical Genetics|February 5, 1998
Comparison of leptin protein levels in Prader-Willi syndrome and control individualsM G Butler, J Moore, A Morawiecki, et al.Cancer Genetics and Cytogenetics|April 1, 1993
Molecular analysis of transforming growth factor beta in giant cell tumor of boneM G Butler, G A Dahir, H S SchwartzAmerican Journal of Medical Genetics. Part A|August 14, 2008
Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) arrayH L Newkirk, D C Bittel, M G ButlerAmerican Journal of Medical Genetics|August 1, 1988
Acrodysostosis: report of a 13-year-old boy with review of literature and metacarpophalangeal pattern profile analysisM G Butler, L J Rames, W B WadlingtonPageof 18