Interstitial Deletions at 6q14.1q15 Associated with Developmental Delay and a Marfanoid Phenotype

Publisher： Karger

E-ISSN： 1661-8777|4|6|280-284

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.4, Iss.6, 2013-08, pp. : 280-284

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

Interstitial Deletions at 6q14.1–q15 Associated with Obesity, Developmental Delay and a Distinct Clinical Phenotype

By  

Molecular Syndromology, Vol. 1, Iss. 2, 2010-06 ,pp. : 75-81

Karger

Access to resources Recommend Favorite

A pure familial 6q15q21 split duplication associated with obesity and transmitted with partial reduction

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1275-1284

John Wiley & Sons Inc

Access to resources Recommend Favorite

Interstitial deletion 5q14.3q21.3 associated with lethal epilepsy

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 4, 2015-04 ,pp. : 866-871

John Wiley & Sons Inc

Access to resources Recommend Favorite

De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 5, 2015-05 ,pp. : 1134-1141

John Wiley & Sons Inc

Access to resources Recommend Favorite

Partial 1q Duplications and Associated Phenotype

By  

Molecular Syndromology, Vol. 6, Iss. 6, 2016-0 ,pp. : 297-303

Karger

Access to resources Recommend Favorite