Authors: DUBA HC ERDEL M LOFFLER J WIRTH J UTERMANN B UTERMANN G

Citation: Hc. Duba et al., NAIL-PATELLA SYNDROME IN A CYTOGENETICALLY BALANCED T(9-17)(Q34.1-Q25) CARRIER, European journal of human genetics, 6(1), 1998, pp. 75-79

Authors: ERDEL M DUBA HC VERDORFER I LINGENHEL A GEIGER R GUTENBERGER KH LUDESCHER E UTERMANN B UTERMANN G

Citation: M. Erdel et al., COMPARATIVE GENOMIC HYBRIDIZATION REVEALS A PARTIAL DE-NOVO TRISOMY 6Q23-QTER IN AN INFANT WITH CONGENITAL-MALFORMATIONS - DELINEATION OF THE PHENOTYPE, Human genetics, 99(5), 1997, pp. 596-601

Authors: DUBA HC WEIRICH HG WEIRICHSCHWAIGER H UTERMANN B NACHBAUR D SOLDER E UTERMANN G

Citation: Hc. Duba et al., CHROMOSOMAL INSTABILITY IN A WOMAN WITH INFERTILITY AND 2 UNAFFECTED BROTHERS - A NEW FAMILIAL CHROMOSOMAL BREAKAGE SYNDROME, Human genetics, 100(3-4), 1997, pp. 431-440

Authors: DUBA HC ERDEL M LOFFLER J BEREUTHER L FISCHER H UTERMANN B UTERMANN G

Citation: Hc. Duba et al., DETECTION OF A DE-NOVO DUPLICATION OF 1Q32-QTER BY FLUORESCENCE IN-SITU HYBRIDIZATION IN A BOY WITH MULTIPLE MALFORMATIONS - FURTHER DELINEATION OF THE TRISOMY 1Q SYNDROME, Journal of Medical Genetics, 34(4), 1997, pp. 309-313

Authors: ERDEL M SCHUFFENHAUER S BUCHHOLZ B BARTHWITTE U KOCHL S UTERMANN B DUBA HC UTERMANN G

Citation: M. Erdel et al., ROUTINE SCREENING FOR MICRODELETIONS BY FISH IN 77 PATIENTS SUSPECTEDOF HAVING PRADER-WILLI OR ANGELMAN SYNDROMES USING YAC CLONE 273A2 (D15S10), Human genetics, 97(6), 1996, pp. 784-793

Authors: ETTL A FELBER S KUNZE C SCHMIDAUER C UTERMANN B DAXER A GOTTINGER W

Citation: A. Ettl et al., HEREDITARY VITREORETINAL DYSTROPHY ASSOCIATED WITH PERIPHERAL NEUROPATHY, Graefe's archive for clinical and experimental ophthalmology, 232(6), 1994, pp. 330-336