Authors: Honour, JW Torresani, T Toublanc, JE Larsson, A Grueters-Kieslich, A Giovanelli, G Donaldson, M Ferrandez-Longas, A Klett, M Hnikova, O Schrama, SMPFDK

Citation: Jw. Honour et al., Procedure for neonatal screening for congenital adrenal hyperplasia due to21-hydroxylase deficiency, HORMONE RES, 55(4), 2001, pp. 201-205

Authors: Marlin, S Blanchard, S Slim, R Lacombe, D Denoyelle, F Alessandri, JL Calzolari, E Drouin-Garraud, V Ferraz, FG Fourmaintraux, A Philip, N Toublanc, JE Petit, C

Citation: S. Marlin et al., Townes-Brocks syndrome: Detection of a SALL1 mutation hot spot and evidence for a position effect in one patient, HUM MUTAT, 14(5), 1999, pp. 377-386

Authors: Toublanc, JE

Citation: Je. Toublanc, Guidelines for neonatal screening programs for congenital hypothyroidism, ACT PAEDIAT, 88, 1999, pp. 13-14

Authors: Toublanc, JE Gruters-Kieslich, A Donaldson, M Ferrandez-Longas, A Giovannelli, G Honour, JW Hnikova, O Klett, M Larsson, A Keizer-Schrama, SMPFD Torresani, T

Citation: Je. Toublanc et al., Revised guidelines for neonatal screening programmes for primary congenital hypothyroidism, HORMONE RES, 52(1), 1999, pp. 49-52

Authors: Toublanc, JE Morgensztejn, F Gendrel, C Boisson-Lesage, C Loria, A

Citation: Je. Toublanc et al., Frequency and severity of hepatic marker alterations in patients with Turner's syndrome, ANN PEDIAT, 46(9), 1999, pp. 565-573