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Results 1 - 9 of 9 for mg
  1. ... Free article on PubMed Central Bittel DC, Butler MG. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular ... PubMed Bittel DC, Kibiryeva N, Talebizadeh Z, Butler MG. Microarray analysis of gene/transcript expression in Prader- ...
  2. ... S, Taudien S, Garber M, Kodira CD, Schueler MG, Shimizu A, Whittaker CA, Chang JL, Cuomo CA, Dewar K, FitzGerald MG, Yang X, Allen NR, Anderson S, Asakawa T, ...
  3. ... Antonarakis SE, DePaulo JR Jr, Ross CA, McInnis MG. Trapping and sequence analysis of 1138 putative exons ... CA, Chang JL, Cuomo CA, Dewar K, FitzGerald MG, Yang X, Abouelleil A, Allen NR, Anderson S, ...
  4. ... Citation on PubMed McKenzie M, Liolitsa D, Hanna MG. Mitochondrial disease: mutations and mechanisms. Neurochem Res. 2004 ... Landon DN, Debono AG, Morgan-Hughes JA, Hanna MG. New phenotypic diversity associated with the mitochondrial tRNA( ...
  5. ... P, Russo S, Gottardi G, Rodeschini O, Atza MG, Natacci F, Larizza L. Small familial supernumerary ring ...
  6. ... Dongen JJ, den Boer ML, Pieters R, Ennas MG, Angelucci E, Koehl U, Greil J, Griesinger F, ...
  7. ... E, Chang JL, Cuomo CA, Eichler E, FitzGerald MG, Jaffe DB, LaButti K, Nicol R, Park HS, ...
  8. ... AD, Martinez E, Massey E, Mawhiney S, Meador MG, Mendez S, Mercado C, Mercado IC, Merritt CE, ...
  9. ... K, Rhodes S, Ridler KA, Schlessinger D, Schueler MG, Sehra HK, Shaw-Smith C, Shen H, Sheridan ...