le syndrome de pierre robin

Gorlin, 1990, 649 Shprintzen, 1992, The implications of the diagnosis of Robin sequence, Cleft Palate Craniofac J, 29, 205, 10.1597/1545-1569(1992)029<0205:TIOTDO>2.3.CO;2 Williams AJ, Williams MA, Walker CA, Bush PG. The Robin anomalad (Pierre Robin syndrome) - a follow-up study. Arch Dis Child 198; 56: 663-8. Sadewitz, 1992, Robin sequence : changes in thinking leading to changes in patient care, Cleft Palate Craniofac J, 29, 246, 10.1597/1545-1569(1992)029<0246:RSCITL>2.3.CO;2 Cohen, 1976, The Robin anomalad : its non-specificity and associated syndromes, J Oral Surg, 34, 587 Cohen, 1999, Robin sequences and complexes: causal heterogeneity and pathogenetic/phenotypic variability, Am J Med Genet, 84, 311, 10.1002/(SICI)1096-8628(19990604)84:4<311::AID-AJMG1>3.0.CO;2-9 Couly, 1988, Le syndrome de Pierre Robin : classification et nouvelle approche thérapeutique, Arch Fr Pediatr, 45, 539 Jean, 1997, Brainstem organisation of swallowing and interaction with respiration. In neural control of the respiratory muscles, Mille AD CRC Press, 223 Abadie, 1993, Le syndrome néonatal de dysfonctionnement du tronc cérébral, Arch Fr Pediatr, 50, 347 Sher, 1992, Mechanisms of airways obstruction in Robin sequence : implications for treatment, Cleft Palate Craniofac J, 29, 224, 10.1597/1545-1569(1992)029<0224:MOAOIR>2.3.CO;2 Baujat, 2001, Oro-esophageal motor disorders in Pierre Robin sequence, J Pediatr Gastroenterol Nutr, 10.1097/00005176-200103000-00012 Sheffield, 1987, A genetic follow-up study of 64 patients with the Pierre Robin complex, Am J Med Genet, 28, 25, 10.1002/ajmg.1320280105