Wolf-Hirschhorn Syndrome with Epibulbar Dermoid: An Unusual Association in a Patient with 4p Deletion and Functional Xp Disomy

Publisher： Karger

E-ISSN： 1424-859x|150|1|17-22

ISSN： 1424-8581

Source： Cytogenetic and Genome Research, Vol.150, Iss.1, 2016-11, pp. : 17-22

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

Submicroscopic Duplication of the Wolf-Hirschhorn Critical Region with a 4p Terminal Deletion

By  

Cytogenetic and Genome Research, Vol. 125, Iss. 2, 2009-08 ,pp. : 103-108

Karger

Access to resources Recommend Favorite

Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome

By  

Cytogenetic and Genome Research, Vol. 91, Iss. 1-4, 2001-01 ,pp. : 81-84

Karger

Access to resources Recommend Favorite

A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p)

By  

Cytogenetic and Genome Research, Vol. 91, Iss. 1-4, 2001-01 ,pp. : 85-89

Karger

Access to resources Recommend Favorite

Posterior Fossa Dermoid Cyst in a Patient with Goldenhar Syndrome

By  

Pediatric Neurosurgery, Vol. 43, Iss. 6, 2007-11 ,pp. : 522-525

Karger

Access to resources Recommend Favorite

Discrepancies in cytogenetic results between different tissues in two fetuses with Wolf- Hirschhorn syndrome

By  

Cytogenetic and Genome Research, Vol. 91, Iss. 1-4, 2001-01 ,pp. : 231-233

Karger

Access to resources Recommend Favorite