Antenatal and Neonatal Screening [Second Edition]Claude Dorche · 2002

Antenatal diagnosis of molybdenum cofactor deficiencyGray, R.George F.; Green, Anne; Nadda Basu, Shishta; Constantine, Glyn; G. Condie, Roy; Dorche, Claude; Vianey-Liaud, Christine; Desjacques, Pierre · American Journal of Obstetrics and Gynecology · 1990

Further Studies on the Nature of Phenylalanine Hydroxylation in BrainAbita, Jean-Pierre; Dorche, Claude; Kaufman, Seymour · Pediatric Research · 1974

Spherophakia associated with molybdenum cofactor deficiencyParini, Rossella; Briscioli, Vincenza; Caruso, Ubaldo; Dorche, Claude; Fortuna, Renato; Minniti, Giuseppe; Selicorni, Angelo; Vismara, Elisabetta; Mancini, Grazia · American Journal of Medical Genetics · 1997

Isolated sulfite oxidase deficiency: identification of 12 novel SUOX mutations in 10 patientsJean L. Johnson; Katharine E. Coyne; Robert M. Garrett; Marie-Therese Zabot; Claude Dorche; Caroline Kisker; K. V. Rajagopalan · 2002

Studies on the interaction of a thiol-dependent hydrogen peroxide scavenging enzyme and phenylalanine hydroxylaseSheldon Milstien; Claude Dorche; Seymour Kaufman · 1990

Genomic structure and mutational spectrum of the bicistronicMOCS1gene defective in molybdenum cofactor deficiency type AJ. Reiss; Ernst Christensen; Gerhard Kurlemann; Marie-Therese Zabot; Claude Dorche · 1998