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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.Cancer Genetics and Cytogenetics|January 1, 1992
Cytogenetic abnormalities in a rare case of giant cell osteogenic sarcomaH S Schwartz, G A Allen, I Chudoba, et al.Cancer Genetics and Cytogenetics|January 1, 1996
Chromosome telomere integrity of human solid neoplasmsM G Butler, M Sciadini, L K Hedges, et al.American Journal of Medical Genetics|July 1, 1987
Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage?M G Butler, B D Hall, R N Maclean, et al.Clinical Genetics|October 7, 2017
Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adultsA M Manzardo, N Weisensel, S Ayala, et al.American Journal of Medical Genetics|September 15, 1993
Metacarpophalangeal pattern profile analysis in Williams syndromeM A Burns, D R McLeod, L R Linton, et al.American Journal of Medical Genetics|January 1, 1988
Metacarpophalangeal pattern profile analysis in Sotos syndrome: a follow-up report on 34 subjectsM G Butler, P F Dijkstra, F J Meaney, et al.Journal of Clinical Pathology|August 1, 1987
Rapid technique of DNA-DNA in situ hybridisation on formalin fixed tissue sections using microwave irradiationP J Coates, P A Hall, M G Butler, et al.Cancer Genetics and Cytogenetics|January 1, 1987
High resolution chromosome and DNA analysis in multiple endocrine neoplasia type II syndromeM G Butler, D R Repaske, G M Joseph, et al.Pageof 18