Literature DB >> 14049206

[DOMINANT HEREDITARY SYNDROME, COMBINING CRANIO-FACIAL DYSOSTOSIS PECULIAR TYPE, GROWTH INSUFFICIENCY OF CHONDRODYSTROPHIC APPEARANCE, AND MASSIVE THICKENING OF OF THE CORTICES OF LONG BONES].

V STANESCO, C MAXIMILIAN, S POENARU, I FLOREA, R STANESCO, V IONESCO, D IOANITIU.   

Abstract

Entities:  

Keywords:  ADOLESCENCE; BONE DISEASES; CHILD; CRANIOFACIAL DYSOSTOSIS; DWARFISM; DYSCHONDROPLASIA; GENETICS, HUMAN; HYPEROSTOSIS, CORTICAL CONGENITAL

Mesh：

Year:  1963        PMID： 14049206

Source DB:  PubMed          Journal:  Rev Fr Endocrinol Clin        ISSN： 0048-8062


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  3 in total

1.  The tricho-dento-osseous (TDO) syndrome.

Authors:  J Lichtenstein; R Warson; R Jorgenson; J P Dorst; V A McKusick
Journal:  Am J Hum Genet       Date:  1972-09       Impact factor: 11.025

Review 2.  Craniotubular bone disorders.

Authors:  R J Gorlin
Journal:  Pediatr Radiol       Date:  1994

3.  Arthrogryposis multiplex congenital in a child manifesting phenotypic features resembling dysosteosclerosis/osteosclerosis malformation complex; 3DCT scan analysis of the skull base.

Authors:  Ali Al Kaissi; Georg Kalchhauser; Franz Grill; Klaus Klaushofer
Journal:  Cases J       Date:  2008-07-23
  3 in total

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