Authors: DAVID D ORTH U HEILBRONNER H GAL A

Citation: D. David et al., A NOVEL SPLICE-SITE MUTATION IN THE CD40L GENE IN A PATIENT WITH X-LINKED HYPER-IGM SYNDROME, Human mutation, 7(2), 1996, pp. 181-182

Authors: DEKOK YJM VOSSENAAR ER CREMERS CWRJ DAHL N LAPORTE J HU LJ LACOMBE D FISCHELGHODSIAN N FRIEDMAN RA PARNES LS THORPE P BITNERGLINDZICZ M PANDER HJ HEILBRONNER H GRAVELINE J DENDUNNEN JT BRUNNER HG ROPERS HH CREMERS FPM

Citation: Yjm. Dekok et al., IDENTIFICATION OF A HOT-SPOT FOR MICRODELETIONS IN PATIENTS WITH X-LINKED DEAFNESS TYPE-3 (DFN3) 900 KB PROXIMAL TO THE DFN3 GENE POU3F4, Human molecular genetics, 5(9), 1996, pp. 1229-1235

Authors: STEIN A HEILBRONNER H JUNGMANN J

Citation: A. Stein et al., SEX-CHROMOSOME ABERRATION WITH A 48,XYYY KARYOTYPE - A CASE-REPORT ONTHE PHENOTYPE OF A RARE SEX-CHROMOSOME COMPLEMENT, Zeitschrift für Kinder- und Jugendpsychiatrie, 22(2), 1994, pp. 130-134

Authors: STEINBACH P WOHRLE D TARIVERDIAN G KENNERKNECHT I BARBI G EDLINGER H ENDERS H GOTZSOTHMANN M HEILBRONNER H HOSENFELD D KIRCHEISEN R MAJEWSKI F MEINECKE P PASSARGE E SCHMIDT A SEIDEL H WOLFF G ZANKL M

Citation: P. Steinbach et al., MOLECULAR ANALYSIS OF MUTATIONS IN THE GENE FMR-1 SEGREGATING IN FRAGILE X-FAMILIES, Human genetics, 92(5), 1993, pp. 491-498