Literature DB >> 4955061

Roentgen differentiation of the oculodentodigital syndrome and the Hallermann-Streiff syndrome in infancy.

G J Kurlander, N W Lavy, J A Campbell.   

Abstract

Entities:  

Mesh:

Year:  1966        PMID: 4955061     DOI: 10.1148/86.1.77

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


× No keyword cloud information.
  8 in total

1.  An autosomal recessive disorder with retardation of growth, mental deficiency, ptosis, pectus excavatum and camptodactyly.

Authors:  F Khaldi; B Bennaceur; A Hammou; M Hamza; H A Gharbi
Journal:  Pediatr Radiol       Date:  1988

2.  Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotype.

Authors:  M A Patton; K M Laurence
Journal:  J Med Genet       Date:  1985-10       Impact factor: 6.318

Review 3.  Craniotubular bone disorders.

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

4.  Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?

Authors:  L A Brueton; S M Huson; B Farren; R M Winter
Journal:  J Med Genet       Date:  1990-03       Impact factor: 6.318

5.  Intrauterine dwarfism, peculiar facies and thin bones with multiple fractures--a new syndrome.

Authors:  K Kozlowski; A Kan
Journal:  Pediatr Radiol       Date:  1988

6.  Osteocraniostenosis.

Authors:  A Verloes; F Narcy; B Grattagliano; A L Delezoide; P Guibaud; J P Schaaps; M Le Merrer; P Maroteaux
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

7.  Wormian bones in osteogenesis imperfecta and other disorders.

Authors:  B Cremin; H Goodman; J Spranger; P Beighton
Journal:  Skeletal Radiol       Date:  1982       Impact factor: 2.199

8.  Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases.

Authors:  Virang Kumar; Natario L Couser; Arti Pandya
Journal:  Case Rep Ophthalmol Med       Date:  2020-04-04
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.