Autor/in Friedrich, Katrin Nürnberg, Gudrun Nürnberg, Peter 2 Baloch, Dost Muhammad 1 Borck, Guntram 1 Daud, Shakeela 1 Eyman, Daniel K 1 Freudenberg, Jan 1 Garcia-F-Villalta, María J 1 Hisama, Fuki M 1 Hoch, Jochen 1 Kakar, Naseebullah 1 Lee, Lin 1 Leistritz, Dru F 1 Lessel, Davor 1 Li, Chumei 1 Oldenburg, Johannes 1 Saha, Bidisha 1 Yilmaz, Rüstem 1 alle zeigenListe einklappen
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group. Borck, Guntram Kakar, Naseebullah Hoch, Jochen Friedrich, Katrin Freudenberg, Jan Nürnberg, Gudrun Yilmaz, Rüstem 2012 - Forschungsinformationssystem des UKE
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations. Friedrich, Katrin Lee, Lin Leistritz, Dru F Nürnberg, Gudrun Saha, Bidisha Hisama, Fuki M Eyman, Daniel K 2010 - Forschungsinformationssystem des UKE
