Collins, E.Treacher: Case with symmetrical congenital notches in outer part of each lower lid and defective development of malar bones. Trans. Ophthal. Soc. D. K.20: 191, July 1900.
7.
Debusmann, Dr.: Familiare kombinierte Gesichtsmissbildung im bereich des ersten Visgeralbogens . Arch. f. Kinderh.120: 133, 1940.
8.
Fernandez, A.O. and Ronis, M.L.: The Treacher Collins syndrome . Arch. Otolaryng.80: 505-519, Nov. 1964 .
9.
Franceschetti, A., Brocher, J.E.W. and Klein, D.: Dysostose mandibulofaciale unilaterale avec deformations multiples du sequelette (processus paramastoids, synostose des vertebres, sacralisation etc.) et torticolis clonique. Ophthalmologica (Basel) 118: 796, 1949.
10.
Fujino, H., Hirsoka, T. and Kyoshoin, Y.: Case report of Treacher Collins syndrome. KyushuJ. Med. Sci.12: 343-346, 1961.
11.
Granrud, H. : On aetiology of dysostosis mandibulo-facialis . Acta Paediat.42: 499, 1953.
12.
Hovels, O.: Sur Pathogenese der Missbildungen des eater Visceralbogens. Ztschr. Kinderh.73: 568, 1953.
13.
Keith. A.Concerning the origin and nature of certain malformations of the face, head, and foot. Brit. J. Surg.28: 173, 1940.
14.
Kibel, M.A. : Mandibulofacial dysostosis (Treacher Collins syndrome). Cent. Afr. J. Med.6: 244-247, June 1960.
15.
Leopold, I.H. , Mahoney, J.F. and Price. M.L.: Symmetric defects in lower lids associated with abnormalities of zygomatic processes and temporal bones. Ophth.34: 210-214, 1945.
16.
Livingstone, G.: Establishment of sound conduction in congenital deformities of external ear. J. Laryng.73: 231, 1958.
17.
Mall, F.P.: On the frequency of localized anomalies in human embryos and infants at birth . Amer. J. Anat.22: 49, 1917.
18.
Mann, I. and Kilner, T.P.: Deficiency of malar bones with defect of lower lids. Brit. J. Ophth.27: 13, 1943.
19.
Maran, A.C.D. : The Treacher Collins syndrome. J. Laryng. and Otology78: 1135, Feb. 1964.
20.
McKenzie, J. and Craig, J.: Mandibulo facial dysostosis (Treacher Collins syndrome). Arch. Dis. Child.30: 391, 1955.
21.
McKenzie, J. : First arch syndrome. Arch. Dis. Child.33: 477, 1958.
22.
Moorehead, P.S., Nowell, P.C., Mellman , W.J., Battips, D.M. and Hungerford , D.A.: Chromosome preparation of leukocytes cultured from human peripheral blood. Exp. Cell Res.20: 613, 1960.
23.
Rogers, B.O. : Berry-Treacher Collins syndrome; a review of 200 cases (mandibulo-facial dysostosis; Franceschetti-Zwahlen syndrome) . Brit. J. Plastic Surg.17: 111, April 1964 .
24.
Rovin, S., Dechi, S.F., Borenstein, D.B. and Cotter, W.B.: Mandibulofacial dysostosis, a familial study of five generations. J. Pediat.65: 215, August 1964.
25.
Wayburne, S. : Mandibulofacial dysostosis in an African infant . Arch. Dis. Child.28: 125, 1953.
26.
Wildervanck, L.S.: Dysostosis mandibulo-facialis (Franceschetti-Zwahlen) in four generations. Acta genet. med. et gem.9: 447, 1960.