Analysis of Turner Syndrome Patients within the Jordanian Population, with a Focus on Four Patients with Y Chromosome Abnormalities

Publisher： Karger

E-ISSN： 1661-5433|7|6|295-302

ISSN： 1661-5425

Source： Sexual Development, Vol.7, Iss.6, 2013-08, pp. : 295-302

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

Three patients with Schaaf–Yang syndrome exhibiting arthrogryposis and endocrinological abnormalities

By  

American Journal Of Medical Genetics Part A, Vol. 176, Iss. 3, 2018-03 ,pp. : 707-711

John Wiley & Sons Inc

Access to resources Recommend Favorite

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome

By Clement-Jones Mark   Schiller Simone  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 695-702

Oxford University Press

Access to resources Recommend Favorite

Clinical spectrum of eye malformations in four patients with Mowat–Wilson syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 7, 2015-07 ,pp. : 1587-1592

John Wiley & Sons Inc

Access to resources Recommend Favorite

Fluorescence in situ Hybridization of psu dic(X)(Xpter-Xq21::Xq21-Xpter) in Two Patients with Turner’s Syndrome

By  

Human Heredity, Vol. 48, Iss. 2, 1998-02 ,pp. : 82-86

Karger

Access to resources Recommend Favorite

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients

By Huppke P.   Laccone F.   Krämer N.   Engel W.   Hanefeld F.  

Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1369-1375

Oxford University Press

Access to resources Recommend Favorite