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Results:
1-7
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Results: 7
Authors:
Tammaa, A
Teich, G
Scholl, T
Salzer, H
Citation: A. Tammaa et al., Ethnic background as a risk factor for gestational diabetes in Central Europe, GEBURTSH FR, 61(3), 2001, pp. 142-146
Authors:
Pyne, MT
Brothman, AR
Ward, B
Pruss, D
Hendrickson, BC
Scholl, T
Citation: Mt. Pyne et al., The BRCA2 genetic variant IVS7+2T -> G is a mutation, J HUM GENET, 45(6), 2000, pp. 351-357
Authors:
Sowers, MF
Scholl, T
Harris, L
Jannausch, M
Citation: Mf. Sowers et al., Bone loss in adolescent and adult pregnant women, OBSTET GYN, 96(2), 2000, pp. 189-193
Authors:
Scholl, T
Citation: T. Scholl, Maryinsky-Ballet, BALLET REV, 27(1), 1999, pp. 7-9
Authors:
Scholl, T
Pyne, MT
Russo, D
Ward, BE
Citation: T. Scholl et al., BRCA1 IVS16+6T -> C is a deleterious mutation that creates an aberrant transcript by activating a cryptic splice donor site, AM J MED G, 85(2), 1999, pp. 113-116
Authors:
Scholl, T
Citation: T. Scholl, The arts of Ballets Russes: The Serge Lifar collection of theater designs,costumes, and paintings at the Wadsworth Atheneum, Hartford, Connecticut, SLAV REV, 58(3), 1999, pp. 721-722
Authors:
Scholl, T
Pyne, MT
Ward, B
Pruss, D
Citation: T. Scholl et al., Biochemical and genetic characterisation shows that the BRCA1 IVS20 insertion is a polymorphism, J MED GENET, 36(7), 1999, pp. 571-572
Risultati:
1-7
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