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7. [Association of male XX with Pierre Robin syndrome in a child whose father has a balanced 46XY, t (16; 17) (p13;q21) translocation]. Petrus M; Bourrouillou G; Dutau G; Colombies P; Rochiccioli P J Genet Hum; 1981 Jun; 29(2):191-6. PubMed ID: 7199077 [TBL] [Abstract][Full Text] [Related]
8. The Stickler syndrome. Opitz JM; France T; Herrmann J; Spranger JW N Engl J Med; 1972 Mar; 286(10):546-7. PubMed ID: 4621768 [No Abstract] [Full Text] [Related]
9. [Pierre Robin syndrome in 2 siblings]. Kołodziejczyk J; Skorochodzki L; Sawicka E Pediatr Pol; 1979 Mar; 54(3):277-80. PubMed ID: 450500 [No Abstract] [Full Text] [Related]
10. Pierre-Robin sequence and severe mental retardation with chaotic behaviour associated with a small interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333)). Vogels A; Haegeman J; Fryns JP Genet Couns; 1997; 8(3):249-52. PubMed ID: 9327270 [TBL] [Abstract][Full Text] [Related]
11. Pierre-Robin anomalad, moderate mental retardation and distal 4q deletion. Fryns JP; Timmermans J; Hoedemaekers J; Emmery L; Van den Berghe H Ann Genet; 1981; 24(3):187-8. PubMed ID: 6974535 [No Abstract] [Full Text] [Related]
12. [Recurrent Pierre-Robin syndrome in a family with translocation (author's transl)]. Ohama K; Takahara H; Kuzumi I; Fujiwara A Jinrui Idengaku Zasshi; 1974 Jun; 19(1):81. PubMed ID: 4476863 [No Abstract] [Full Text] [Related]
13. [Dystopia and laryngeal malformation in a child with Treacher Collins and Pierre Robin syndromes]. Poliakov AA Vestn Otorinolaringol; 1996; (5):36. PubMed ID: 8999645 [No Abstract] [Full Text] [Related]
14. Pierre-Robin syndrome: a case report. Chiriac A; Dawson A; Krapp M; Axt-Fliedner R Arch Gynecol Obstet; 2008 Jan; 277(1):95-8. PubMed ID: 17618445 [TBL] [Abstract][Full Text] [Related]
15. [Pierre Robin syndrome in the light of our observations]. Holendzki Z; Chmielewska J; Koczela A Pol Tyg Lek; 1975 Jul; 30(27):1147-9. PubMed ID: 1135105 [No Abstract] [Full Text] [Related]
16. Presentation of the isochromosome trisomy 18 syndrome in an infant with the Robin anomalad. Wiswell TE; Edwards RG Hawaii Med J; 1986 May; 45(5):126-7. PubMed ID: 3721853 [No Abstract] [Full Text] [Related]
17. Robin sequences and complexes: causal heterogeneity and pathogenetic/phenotypic variability. Cohen MM Am J Med Genet; 1999 Jun; 84(4):311-5. PubMed ID: 10340643 [TBL] [Abstract][Full Text] [Related]
18. [3 cases of Pierre Robin syndrome]. Spada A; Ambrosiana S Arch Sci Med (Torino); 1969 Apr; 126(4):195-200. PubMed ID: 17342890 [TBL] [Abstract][Full Text] [Related]
19. Pierre Robin syndrome: an update. Olasoji HO; Ambe PJ; Adesina OA Niger Postgrad Med J; 2007 Jun; 14(2):140-5. PubMed ID: 17599114 [TBL] [Abstract][Full Text] [Related]
20. Cerebro-costo-mandibular syndrome: a follow-up study with 6 patients. Schrander-Stumpel C; van der Meer S; De Die-Smulders C; Meinecke P; Rupprecht E; Maroteaux P; Schrander J; Fryns JP Genet Couns; 1996; 7(1):71-2. PubMed ID: 8652092 [No Abstract] [Full Text] [Related] [Next] [New Search]