AAAAAA
Results: 26-32/32
Authors:
Buiting, K
Korner, C
Ulrich, B
Wahle, E
Horsthemke, B
Citation: K. Buiting et al., The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11 -> q13, CYTOG C GEN, 87(1-2), 1999, pp. 125-131
Authors:
Zeschnigk, M
Lohmann, D
Horsthemke, B
Citation: M. Zeschnigk et al., A PCR test for the detection of hypermethylated alleles at the retinoblastoma locus, J MED GENET, 36(10), 1999, pp. 793-794
Authors:
Schomburg, L
Turwitt, S
Prescher, G
Lohmann, D
Horsthemke, B
Bauer, K
Citation: L. Schomburg et al., Human TRH-degrading ectoenzyme - cDNA cloning, functional expression, genomic structure and chromosomal assignment, EUR J BIOCH, 265(1), 1999, pp. 415-422
Authors:
Buiting, K
Dittrich, B
Dworniczak, B
Lerer, I
Abeliovich, D
Cottrell, S
Temple, IK
Harvey, JF
Lich, C
Gross, S
Horsthemke, B
Citation: K. Buiting et al., A 28-kb deletion spanning D15S63 (PW71) in five families: A rare neutral variant?, AM J HU GEN, 65(6), 1999, pp. 1588-1594
Authors:
Ohta, T
Buiting, K
Kokkonen, H
McCandless, S
Heeger, S
Leisti, H
Driscoll, DJ
Cassidy, SB
Horsthemke, B
Nicholls, RD
Citation: T. Ohta et al., Molecular mechanism of Angelman syndrome in two large families involves animprinting mutation, AM J HU GEN, 64(2), 1999, pp. 385-396
Authors:
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
Citation: T. Ohta et al., Imprinting-mutation mechanisms in Prader-Willi syndrome, AM J HU GEN, 64(2), 1999, pp. 397-413
Authors:
Klutz, M
Horsthemke, B
Lohmann, DR
Citation: M. Klutz et al., RB1 gene mutations in peripheral blood DNA of patients with isolated unilateral retinoblastoma, AM J HU GEN, 64(2), 1999, pp. 667-668