Additional patients with 4q deletion: Severe growth delay and polycystic kidney disease associated with 4q21q22 loss

Publisher： John Wiley & Sons Inc

E-ISSN： 1442-200x|57|5|880-883

ISSN： 1328-8067

Source： PEDIATRICS INTERNATIONAL, Vol.57, Iss.5, 2015-10, pp. : 880-883

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

An Interstitial 4q31.21q31.22 Microdeletion Associated with Developmental Delay: Case Report and Literature Review

By  

Cytogenetic and Genome Research, Vol. 142, Iss. 4, 2014-04 ,pp. : 227-238

Karger

Access to resources Recommend Favorite

22q11.2 deletion syndrome presenting with early‐onset Parkinson's disease

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 9, 2015-08 ,pp. : 1289-1290

John Wiley & Sons Inc

Access to resources Recommend Favorite

Autoimmunity and regulatory T cells in 22q11.2 deletion syndrome patients

By  

PEDIATRIC ALLERGY AND IMMUNOLOGY, Vol. 26, Iss. 6, 2015-09 ,pp. : 591-594

John Wiley & Sons Inc

Access to resources Recommend Favorite

Assignment1 of KPNA4 and KPNB1 encoding karyopherin alpha 4 and beta 1 to human chromosome bands 11q22 and 17q21 respectively, by in situ hybridization

By  

Cytogenetic and Genome Research, Vol. 89, Iss. 3-4, 2000-08 ,pp. : 258-259

Karger

Access to resources Recommend Favorite

Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay

By  

Cytogenetic and Genome Research, Vol. 145, Iss. 1, 2015-04 ,pp. : 19-24

Karger

Access to resources Recommend Favorite