A previously undescribed de novo 4p15 deletion in a patient with apparently isolated metopic craniosynostosis

Publisher： John Wiley & Sons Inc

E-ISSN： 1552-4833|155|10|2543-2551

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.155, Iss.10, 2011-10, pp. : 2543-2551

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

De novo 4q duplication/deletion in a fetus with a congenital heart defect

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 8, 2015-08 ,pp. : 1932-1936

John Wiley & Sons Inc

Access to resources Recommend Favorite

A maternally inherited 16p13.11‐p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1315-1322

John Wiley & Sons Inc

Access to resources Recommend Favorite

Chromosome 1p31.1p31.3 Deletion in a Patient with Craniosynostosis, Central Nervous System and Renal Malformation: Case Report and Review of the Literature

By  

Molecular Syndromology, Vol. 8, Iss. 1, 2016-11 ,pp. : 30-35

Karger

Access to resources Recommend Favorite

Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder

By  

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics, Vol. 168, Iss. 4, 2015-06 ,pp. : 258-264

John Wiley & Sons Inc

Access to resources Recommend Favorite

De novo 15.5-Mb Interstitial Deletion in 5p in a Male Ascertained by Oligospermia

By  

Molecular Syndromology, Vol. 4, Iss. 5, 2013-06 ,pp. : 250-254

Karger

Access to resources Recommend Favorite