Treacher Collins syndrome-Reference-Cited by-同舟云学术

Treacher Collins syndrome

Published:1996-09 Issue:Supplement_1 Volume:5 Page:1391-1393
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Dixon Michael J.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/5/Supplement_1/1391/1882256/5-Supplement_1-1391.pdf

Reference57 articles.

1. Notice of several cases of malformation of the external ear, together with experiments on the state of hearing in such persons;Thomson;Monthly J. Med. Sci.,1846

2. Cases with symmetrical congenital notches in the outer part of each lid and defective development of the malar bones;Treacher Collins;Trans. Ophthalmol. Soc. UK,1900

3. Mandibulo-facial dysostosis: New hereditary syndrome;Franceschetti;Acta. Ophthalmol.,1949

4. Older paternal age and fresh gene mutation: data on additional disorders;Jones;J. Pediatr.,1975

5. The ear deformities in mandibulofacial dysostosis;Phelps;Clin. Otolaryngol.,1981

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1. Bilateral Internal Carotid Artery Hypoplasia with Craniofacial Anomalies: A Case of Suspected Treacher Collins Syndrome;NMC Case Report Journal;2023-12-31

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3. The etiology, clinical features, and treatment options of hemifacial microsomia;Oral Diseases;2023-03-13

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