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6. Mandibulofacial dysostosis (Treacher-Collins syndrome) in the fetus: novel association with Pectus carinatum in a molecularly confirmed case and review of the fetal phenotype. Konstantinidou AE; Tasoulas J; Kallipolitis G; Gasparatos S; Velissariou V; Paraskevakou H Birth Defects Res A Clin Mol Teratol; 2013 Dec; 97(12):774-80. PubMed ID: 24288143 [TBL] [Abstract][Full Text] [Related]
9. Treacher-Collins syndrome: an association with polyhydramnios. Kopelman JN; Duff P Mil Med; 1988 Sep; 153(9):485-6. PubMed ID: 3141842 [No Abstract] [Full Text] [Related]
10. The hutterite variant of Treacher Collins syndrome: a 28-year-old story solved. Caluseriu O; Lowry BR; McLeod R; Lamont R; Parboosingh JS; Bernier FP; Innes AM Am J Med Genet A; 2013 Nov; 161A(11):2855-9. PubMed ID: 24108658 [TBL] [Abstract][Full Text] [Related]
11. Genital anomalies in a patient with Treacher Collins syndrome. Writzl K; Jeruc J; Oldridge M; Peterlin B; Hennekam RC Am J Med Genet A; 2008 Aug; 146A(16):2169-71. PubMed ID: 18627048 [No Abstract] [Full Text] [Related]
12. Delayed-onset infantile cataracts in a case of Treacher Collins syndrome. Biebesheimer JB; Fredrick DR Arch Ophthalmol; 2004 Nov; 122(11):1721-2. PubMed ID: 15534141 [No Abstract] [Full Text] [Related]
13. [Inguinal hernia, hydrocele, umbilical cyst and osseous manifestations in Berry-Treacher Collins syndrome (mandibulofacial dysostosis-FranceschettZwahlen-Klein syndrome). Case report and review of the literature]. Saidi M; Chagnon J Union Med Can; 1970 May; 99(5):882-90. PubMed ID: 5450383 [No Abstract] [Full Text] [Related]
15. Hearing loss in the Treacher-Collins syndrome. Marres HA Adv Otorhinolaryngol; 2002; 61():209-15. PubMed ID: 12408086 [TBL] [Abstract][Full Text] [Related]
16. Craniofacial disorders that have phenotypic overlap with Treacher Collins syndrome. Green B; Nikkhah D; Cobb AR; Dunaway DJ J Plast Reconstr Aesthet Surg; 2013 Aug; 66(8):e234-5. PubMed ID: 23664577 [No Abstract] [Full Text] [Related]
17. Co-occurrence of Down syndrome and Treacher-Collins syndrome. Sonoda T; Sawada K; Kouno K; Takagi J; Ikeda T; Sameshima H; Ikenoue T Pediatr Int; 2002 Aug; 44(4):440-2. PubMed ID: 12139573 [No Abstract] [Full Text] [Related]
18. Hereditary macrostomus in the rabbit: a model for Treacher Collins syndrome, one form of mandibulofacial dysostosis. Fox RR; Crary DD J Hered; 1979; 70(6):369-72. PubMed ID: 544686 [TBL] [Abstract][Full Text] [Related]
19. Cleft palate, bilateral external auditory canal atresia, and other midline defects associated with Diamond-Blackfan anemia: case report. McFarren A; Jayabose S; Fevzi Ozkaynak M; Tugal O; Sandoval C J Pediatr Hematol Oncol; 2007 May; 29(5):338-40. PubMed ID: 17483715 [TBL] [Abstract][Full Text] [Related]