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Results: 1-13 |
Results: 13
Bardet-Biedl syndrome - aspects of nephro-urology and human genetics.
Authors: Bruhl, P Schwanitz, G Mallmann, R Muller, SC Raff, R
Citation: P. Bruhl et al., Bardet-Biedl syndrome - aspects of nephro-urology and human genetics., KLIN PADIAT, 213(1), 2001, pp. 8-12
Cytogenetic and andrological status and ICSI-results in couples with severe male factor infertility
Authors: Haidl, G Peschka, B Schwanitz, G Montag, M van der Ven, K van der Ven, H
Citation: G. Haidl et al., Cytogenetic and andrological status and ICSI-results in couples with severe male factor infertility, ASIAN J AND, 2(4), 2000, pp. 293-296
Combination of hypospadias and maldescended testis as cardinal symptoms ingonosomal chromosome aberrations
Authors: Raff, R Schubert, R Schwanitz, G van der Ven, K Bruhl, P
Citation: R. Raff et al., Combination of hypospadias and maldescended testis as cardinal symptoms ingonosomal chromosome aberrations, EUR J PED S, 10(4), 2000, pp. 270-275
Gerhard Koch 1913-1999 - In memoriam
Authors: Schwanitz, G Gebhart, E Rott, HD
Citation: G. Schwanitz et al., Gerhard Koch 1913-1999 - In memoriam, AM J MED G, 95(3), 2000, pp. 191-192
Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2
Authors: Trost, D Wiebe, W Uhlhaas, S Schwindt, P Schwanitz, G
Citation: D. Trost et al., Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2, J MED GENET, 37(6), 2000, pp. 452-454
Formation of uniparental disomy 7 delineated from new cases and a UPD7 case after trisomy 7 rescue. Presentation of own results and review of the literature
Authors: Mergenthaler, S Wollmann, HA Burger, B Eggermann, K Kaiser, P Ranke, MB Schwanitz, G Eggermann, T
Citation: S. Mergenthaler et al., Formation of uniparental disomy 7 delineated from new cases and a UPD7 case after trisomy 7 rescue. Presentation of own results and review of the literature, ANN GENET, 43(1), 2000, pp. 15-21
Congenital cardiovascular malformations and chromosomal microdeletions in 22q11.2
Authors: Trost, D Engels, H Bauriedel, G Wiebe, W Schwanitz, G
Citation: D. Trost et al., Congenital cardiovascular malformations and chromosomal microdeletions in 22q11.2, DEUT MED WO, 124(1-2), 1999, pp. 3-7
Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injection
Authors: Peschka, B Leygraaf, J van der Ven, K Montag, M Schartmann, B Schubert, R van der Ven, H Schwanitz, G
Citation: B. Peschka et al., Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injection, HUM REPR, 14(9), 1999, pp. 2257-2263
Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping
Authors: Peschka, B Leygraaf, J Hansmann, D Hansmann, M Schrock, E Ried, T Engels, H Schwanitz, G Schubert, R
Citation: B. Peschka et al., Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping, PRENAT DIAG, 19(12), 1999, pp. 1143-1149
Partial trisomy 2 due to unbalanced transmission of a maternal translocation 2/15 in a child after IVF treatment
Authors: Leygraaf, J Schwanitz, G Raff, R van der Ven, K
Citation: J. Leygraaf et al., Partial trisomy 2 due to unbalanced transmission of a maternal translocation 2/15 in a child after IVF treatment, GEBURTSH FR, 59(5), 1999, pp. 232-234
Characterisation, phenotypic manifestations and X-inactivation pattern in 14 patients with X-autosome translocations
Authors: Kalz-Fuller, B Sleegers, E Schwanitz, G Schubert, R
Citation: B. Kalz-fuller et al., Characterisation, phenotypic manifestations and X-inactivation pattern in 14 patients with X-autosome translocations, CLIN GENET, 55(5), 1999, pp. 362-366
Formation of supernumerary euchromatic short arm isochromosomes: Parent and cell stage of origin in new cases and review of the literature
Authors: Eggermann, T Schubert, R Engels, H Apacik, C Stengel-Rutkowski, S Haefliger, C Emiliani, V Ricagni, C Schwanitz, G
Citation: T. Eggermann et al., Formation of supernumerary euchromatic short arm isochromosomes: Parent and cell stage of origin in new cases and review of the literature, ANN GENET, 42(2), 1999, pp. 75-80
A case of de novo translocation 16;21: Trisomy 16q phenotype and origin ofthe aberration.
Authors: Eggermann, T Kolin-Gerresheim, I Gerresheim, F Schwanitz, G
Citation: T. Eggermann et al., A case of de novo translocation 16;21: Trisomy 16q phenotype and origin ofthe aberration., ANN GENET, 41(4), 1998, pp. 205-208
Risultati: 1-13 |