Literature DB >> 4833883

Cleidocranial dysostosis. A review of 40 new cases.

J L Jarvis, T E Keats.   

Abstract

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Year:  1974        PMID: 4833883     DOI: 10.2214/ajr.121.1.5

Source DB:  PubMed          Journal:  Am J Roentgenol Radium Ther Nucl Med        ISSN: 0002-9580


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  17 in total

1.  Cleidocranial dysplasia: complete clinical, radiological and histological profiles.

Authors:  Ruchieka Vij; Puneet Batra; Hitesh Vij
Journal:  BMJ Case Rep       Date:  2013-03-20

2.  Further delineation of the Yunis-Varon syndrome.

Authors:  R C Hennekam; C Vermeulen-Meiners
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

Review 3.  Cleidocranial dysplasia: clinical and molecular genetics.

Authors:  S Mundlos
Journal:  J Med Genet       Date:  1999-03       Impact factor: 6.318

4.  Cleidocranial dysplasia.

Authors:  Ramakant Dixit; Kalpana Dixit; A R Paramez
Journal:  Lung India       Date:  2010-07

5.  Cleidocranial dysplasia: a rare cause of disproportionate severe short stature.

Authors:  Manzoor Ahmad Bhat; Bashir Ahmad Laway; Suhail Mantoo; Khalid Choudry; Suman Kotwal; Shahnaz Ahmad Mir
Journal:  Oman Med J       Date:  2012-09

6.  Congenital pseudarthrosis of the clavicle.

Authors:  Guido Currarino; John A Herring
Journal:  Pediatr Radiol       Date:  2009-09-09

7.  A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.

Authors:  G J Feldman; N H Robin; L A Brueton; E Robertson; E M Thompson; J Siegel-Bartelt; D L Gasser; L C Bailey; E H Zackai; M Muenke
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025

8.  Histological examination and clinical evaluation of the jawbone of an adult patient with cleidocranial dysplasia: a case report.

Authors:  Sigmar Schnutenhaus; Ralph G Luthardt; Heike Rudolph; Werner Götz
Journal:  Int J Clin Exp Pathol       Date:  2015-07-01

9.  Cleidocranial dysplasia syndrome: clinical characteristics and mutation study of a Chinese family.

Authors:  Shengguo Wang; Shu Zhang; Yanmin Wang; Yangxi Chen; Li Zhou
Journal:  Int J Clin Exp Med       Date:  2013-10-25

10.  Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations.

Authors:  Taketoshi Yoshida; Hirokazu Kanegane; Motomi Osato; Masatoshi Yanagida; Toshio Miyawaki; Yoshiaki Ito; Katsuya Shigesada
Journal:  Am J Hum Genet       Date:  2002-08-26       Impact factor: 11.025

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