Authors: Hertz, JM Juncker, I Persson, U Matthijs, G Schmidtke, J Petersen, MB Kjeldsen, M Gregersen, N

Citation: Jm. Hertz et al., Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome, HUM MUTAT, 18(2), 2001, pp. 141-148

Authors: Borglum, AD Balslev, T Haagerup, A Birkebaek, N Binderup, H Kruse, TA Hertz, JM

Citation: Ad. Borglum et al., A new locus for Seckel syndrome on chromosome 18p11.31-q11.2, EUR J HUM G, 9(10), 2001, pp. 753-757

Authors: Jais, JP Knebelmann, B Giatras, I De Marchi, M Rizzoni, G Renieri, A Weber, M Gross, O Netzer, KO Flinter, F Pirson, Y Verellen, C Wieslander, J Persson, U Tryggvason, K Martin, P Hertz, JM Schroder, C Sanak, M Krejcova, S Carvalho, MF Saus, J Antignac, C Smeets, H Gubler, MC

Citation: Jp. Jais et al., X-linked Alport syndrome: Natural history in 195 families and genotype-phenotype correlations in males, J AM S NEPH, 11(4), 2000, pp. 649-657

Authors: Haagerup, A Hertz, JM Christensen, MF Binderup, H Kruse, TA

Citation: A. Haagerup et al., Cathepsin K gene mutations and 1q21 haplotypes in patients with pycnodysostosis in an outbred population, EUR J HUM G, 8(6), 2000, pp. 431-436

Authors: Kamperis, K Siggaard, C Herlin, T Nathan, E Hertz, JM Rittig, S

Citation: K. Kamperis et al., A novel splicing mutation in the V-2 vasopressin receptor, PED NEPHROL, 15(1-2), 2000, pp. 43-49

Authors: Hertz, JM Schell, G Doerfler, W

Citation: Jm. Hertz et al., Factors affecting de novo methylation of foreign DNA in mouse embryonic stem cells, J BIOL CHEM, 274(34), 1999, pp. 24232-24240