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Results:
1-8
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Results: 8
Authors:
Hannula, K
Lipsanen-Nyman, M
Scherer, SW
Holmberg, C
Hoglund, P
Kere, J
Citation: K. Hannula et al., Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNA, GENOMICS, 73(1), 2001, pp. 1-9
Authors:
Taskinen, M
Saarinen-Pihkala, U
Hovi, L
Lipsanen-Nyman, M
Citation: M. Taskinen et al., Syndrome X in testicular-cancer survivors - Authors' reply, LANCET, 357(9251), 2001, pp. 229-229
Authors:
Hannula, K
Kere, J
Pirinen, S
Holmberg, C
Lipsanen-Nyman, M
Citation: K. Hannula et al., Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?, J MED GENET, 38(4), 2001, pp. 273-278
Authors:
Hannula, K
Lipsanen-Nyman, M
Kontiokari, T
Kere, J
Citation: K. Hannula et al., A narrow segment of maternal uniparental disomy of chromosome 7q31-qter inSilver-Russell syndrome delimits a candidate gene region, AM J HU GEN, 68(1), 2001, pp. 247-253
Authors:
Avela, K
Lipsanen-Nyman, M
Idanheimo, N
Seemanova, E
Rosengren, S
Makela, TP
Perheentupa, J
de la Chapelle, A
Lehesjoki, AE
Citation: K. Avela et al., Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism, NAT GENET, 25(3), 2000, pp. 298-301
Authors:
Taskinen, M
Saarinen-Pihkala, UM
Hovi, L
Lipsanen-Nyman, M
Citation: M. Taskinen et al., Impaired glucose tolerance and dyslipidaemia as late effects after bone-marrow transplantation in childhood, LANCET, 356(9234), 2000, pp. 993-997
Authors:
Lehto, M
Wipemo, C
Ivarsson, SA
Lindgren, C
Lipsanen-Nyman, M
Weng, J
Wibell, L
Widen, E
Tuomi, T
Groop, L
Citation: M. Lehto et al., High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes, DIABETOLOG, 42(9), 1999, pp. 1131-1137
Authors:
Kivitie-Kallio, S
Eronen, M
Lipsanen-Nyman, M
Marttinen, E
Norio, R
Citation: S. Kivitie-kallio et al., Cohen syndrome: evaluation of its cardiac, endocrine and radiological features, CLIN GENET, 56(1), 1999, pp. 41-50
Risultati:
1-8
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