Clinical and Radiological Characteristics of 22 Children with SHOX Anomalies and Familial Short Stature Suggestive of Léri-Weill Dyschondrosteosis

Publisher： Karger

E-ISSN： 1663-2826|76|3|178-185

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.76, Iss.3, 2011-09, pp. : 178-185

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Radiological Signs of Leri-Weill Dyschondrosteosis in Turner Syndrome

By  

Hormone Research in Paediatrics, Vol. 55, Iss. 2, 2001-08 ,pp. : 71-76

Karger

Access to resources Recommend Favorite

SHOX in Short Stature Syndromes

By  

Hormone Research in Paediatrics, Vol. 55, Iss. 1, 2004-11 ,pp. : 21-23

Karger

Access to resources Recommend Favorite

Short Stature before Puberty: Which Children Should Be Screened for SHOX Deficiency?

By  

Hormone Research in Paediatrics, Vol. 80, Iss. 4, 2013-09 ,pp. : 273-280

Karger

Access to resources Recommend Favorite

Trisomy of the Short Stature Homeobox-Containing Gene (SHOX) due to Duplication/Deletion of the X Chomosome: Clinical Implications on the Stature

By  

Hormone Research in Paediatrics, Vol. 74, Iss. 4, 2010-08 ,pp. : 297-304

Karger

Access to resources Recommend Favorite

Radiological Features in Patients with Short Stature Homeobox-Containing (SHOX) Gene Deficiency and Turner Syndrome before and after 2 Years of GH Treatment

By  

Hormone Research in Paediatrics, Vol. 84, Iss. 1, 2015-05 ,pp. : 14-25

Karger

Access to resources Recommend Favorite