Authors:
Runte, M
Farber, C
Lich, C
Zeschnigk, M
Buchholz, T
Smith, A
Van Maldergem, L
Burger, J
Muscatelli, F
Gillessen-Kaesbach, G
Horsthemke, B
Buiting, K
Citation: M. Runte et al., Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15, EUR J HUM G, 9(7), 2001, pp. 519-526
Authors:
Dorr, S
Midro, AT
Farber, C
Giannakudis, J
Hansmann, I
Citation: S. Dorr et al., Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24, GENOMICS, 71(2), 2001, pp. 174-181
Authors:
Farber, C
Gross, S
Neesen, J
Buiting, K
Horsthemke, B
Citation: C. Farber et al., Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15, GENOMICS, 65(2), 2000, pp. 174-183
Authors:
Buiting, K
Farber, C
Kroisel, P
Wagner, K
Brueton, L
Robertson, ME
Lich, C
Horsthemke, B
Citation: K. Buiting et al., Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselling, CLIN GENET, 58(4), 2000, pp. 284-290
Authors:
Farber, C
Dittrich, B
Buiting, K
Horsthemke, B
Citation: C. Farber et al., The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion, HUM MOL GEN, 8(2), 1999, pp. 337-343