Literature DB >> 1847948

Prenatal ultrasonic diagnosis of mandibulofacial dysostosis (Treacher Collins syndrome).

I Meizner1, R Carmi, M Katz.   

Abstract

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Year:  1991        PMID： 1847948     DOI： 10.1002/jcu.1870190213

Source DB:  PubMed          Journal:  J Clin Ultrasound        ISSN： 0091-2751            Impact factor:   0.910


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  5 in total

1.  Prenatal evaluation of the middle ear and diagnosis of middle ear hypoplasia using MRI.

Authors:  Eldad Katorza; Catherine Nahama-Allouche; Vanina Castaigne; Marie Gonzales; Eva Galliani; Sandrine Marlin; Jean-Marie Jouannic; Jonathan Rosenblatt; Hubert Ducou le Pointe; Catherine Garel
Journal:  Pediatr Radiol       Date:  2010-12-08

2.  The mutational spectrum in Treacher Collins syndrome reveals a predominance of mutations that create a premature-termination codon.

Authors:  S J Edwards; A J Gladwin; M J Dixon
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

Review 3.  Treacher Collins syndrome.

Authors:  M J Dixon
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

4.  Prenatal diagnosis of treacher-collins syndrome using three-dimensional ultrasonography and differential diagnosis with other acrofacial dysostosis syndromes.

Authors:  Daniela Cardoso Pereira; Luiz Claudio Silva Bussamra; Edward Araujo Júnior; Carolina Leite Drummond; Luciano Marcondes Machado Nardozza; Antonio Fernandes Moron; José Mendes Aldrighi
Journal:  Case Rep Obstet Gynecol       Date:  2013-04-04

5.  Franceschetti syndrome.

Authors:  Vikrant Kasat
Journal:  Contemp Clin Dent       Date:  2011-07
  5 in total

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