Partial hexasomy 15pter→15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report

Por Nietzel, A, Albrecht, B, Starke, H, Heller, A, Gillessen-Kaesbac..., G, Claussen, U, Liehr, T
Publicado em 2003

Internal fluorescence labeling with fluorescent deoxynucleotides in two-label peak-height encoded DNA sequencing by capillary electrophoresis.

Por Starke, H R, Yan, J Y, Zhang, J Z, Mühlegger, K, Effgen, K, Dovichi, N J
Publicado em 1994

Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH

Por Stankiewicz, P., Bocian, E., Jakubow-Durska, K., Obersztyn, E., Lato, E., Starke, H., Mroczek, K., Mazurczak, T.
Publicado em 2000

Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11→q11:)/46,XX karyotype

Por von Eggeling, F, Hoppe, C, Bartz, U, Starke, H, Houge, G, Claussen, U, Ernst, G, Kotzot, D, Liehr, T
Publicado em 2002

Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes

Por Weise, A, Starke, H, Heller, A, Tonnies, H, Volleth, M, Stumm, M, Gabriele, S, Nietzel, A, Claussen, U, Liehr, T
Publicado em 2002

Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review

Por Heller, A., Seidel, J, Hubler, A, Starke, H, Beensen, V, Senger, G, Rocchi, M, Wirth, J, Chudoba, I, Claussen, U, Liehr, T
Publicado em 2000