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Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
Saitoh S, Buiting K, Cassidy SB, Conroy JM, Driscoll DJ, Gabriel JM, Gillessen-Kaesbach G, Glenn CC, Greenswag LR, Horsthemke B, Kondo I, Kuwajima K, Niikawa N, Rogan PK, Schwartz S, Seip J, Williams CA, Nicholls RD. Saitoh S, et al. Among authors: gabriel jm. Am J Med Genet. 1997 Jan 20;68(2):195-206. Am J Med Genet. 1997. PMID: 9028458
Imprinting-mutation mechanisms in Prader-Willi syndrome.
Ohta T, Gray TA, Rogan PK, Buiting K, Gabriel JM, Saitoh S, Muralidhar B, Bilienska B, Krajewska-Walasek M, Driscoll DJ, Horsthemke B, Butler MG, Nicholls RD. Ohta T, et al. Among authors: gabriel jm. Am J Hum Genet. 1999 Feb;64(2):397-413. doi: 10.1086/302233. Am J Hum Genet. 1999. PMID: 9973278 Free PMC article.
A model system to study genomic imprinting of human genes.
Gabriel JM, Higgins MJ, Gebuhr TC, Shows TB, Saitoh S, Nicholls RD. Gabriel JM, et al. Proc Natl Acad Sci U S A. 1998 Dec 8;95(25):14857-62. doi: 10.1073/pnas.95.25.14857. Proc Natl Acad Sci U S A. 1998. PMID: 9843980 Free PMC article.
Report of the fourth international workshop on human chromosome 15 mapping 1997.
Morton CC, Christian SL, Donlon TA, Driscoll DJ, Fink JK, Gabriel JM, Gotway G, Greally JM, Hitchins MP, Howard HC, Ji Y, Leonard S, Lerner T, Magenis E, Malcolm S, Ohta T, Rainier S, Rees M, Riley B, Robinson WP, Saitoh S, Schultz R, Sell S, Sharp JD, Nicholls RD, et al. Morton CC, et al. Among authors: gabriel jm. Cytogenet Cell Genet. 1999;84(1-2):12-21. doi: 10.1159/000015203. Cytogenet Cell Genet. 1999. PMID: 10343092 No abstract available.
Molecular cloning of a candidate chicken prion protein.
Gabriel JM, Oesch B, Kretzschmar H, Scott M, Prusiner SB. Gabriel JM, et al. Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9097-101. doi: 10.1073/pnas.89.19.9097. Proc Natl Acad Sci U S A. 1992. PMID: 1409608 Free PMC article.
75 results