Literature DB >> 18142195

The mandibulofacial dysostosis; a new hereditary syndrome.

A FRANCESCHETTI, D KLEIN.   

Abstract

Entities:  

Keywords:  FACE/abnormalities; JAWS/deformities

Mesh：

Year:  1949        PMID： 18142195

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN： 0001-639X


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  26 in total

1.  [The eye and craniofacial dysostosis].

Authors:  P VANCEA; G BARBU; P P VANCEA; P CERNEA
Journal:  Albrecht Von Graefes Arch Ophthalmol       Date:  1961

Review 2.  Craniofacial birth defects: The role of neural crest cells in the etiology and pathogenesis of Treacher Collins syndrome and the potential for prevention.

Authors:  Paul A Trainor
Journal:  Am J Med Genet A       Date:  2010-08-23       Impact factor: 2.802

Review 3.  Treacher Collins syndrome: clinical implications for the paediatrician--a new mutation in a severely affected newborn and comparison with three further patients with the same mutation, and review of the literature.

Authors:  Jan-Ulrich Schlump; Anja Stein; Ute Hehr; Tanja Karen; Claudia Möller-Hartmann; Nursel H Elcioglu; Nadja Bogdanova; Hartmut Fritz Woike; Dietmar R Lohmann; Ursula Felderhoff-Mueser; Annette Linz; Dagmar Wieczorek
Journal:  Eur J Pediatr       Date:  2012-06-23       Impact factor: 3.183

Review 4.  Facial dysostoses: Etiology, pathogenesis and management.

Authors:  Paul A Trainor; Brian T Andrews
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-10-04       Impact factor: 3.908

Review 5.  Syndromes of the first and second branchial arches, part 2: syndromes.

Authors:  J M Johnson; G Moonis; G E Green; R Carmody; H N Burbank
Journal:  AJNR Am J Neuroradiol       Date:  2010-04-01       Impact factor: 3.825

6.  TREACHER-COLLINS SYNDROME: A Case Report.

Authors:  A Ravikumar
Journal:  Med J Armed Forces India       Date:  2017-06-26

7.  [Defects and excess in Laurence-Moon-Bardet-Biedl syndrome].

Authors:  G Jacobi
Journal:  Z Kinderheilkd       Date:  1965-10-11

Review 8.  Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disorders.

Authors:  Paul A Trainor; Amy E Merrill
Journal:  Biochim Biophys Acta       Date:  2013-11-16

9.  Severe fetal manifestation of hemifacial microsomia.

Authors:  B Putz; H Rehder; R Grosspietzsch
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1980

10.  Postaxial acrofacial dysostosis or Miller syndrome. A case report.

Authors:  D Barbuti; C Orazi; A Reale; C Paradisi
Journal:  Eur J Pediatr       Date:  1989-02       Impact factor: 3.183
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