3p14 deletion is a rare contiguous gene syndrome: Report of 2 new patients and an overview of 14 patients

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1223-1230

John Wiley & Sons Inc

Access to resources Recommend Favorite

22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review

By  

Molecular Syndromology, Vol. 2, Iss. 1, 2011-12 ,pp. : 35-44

Karger

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

De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: A case report and a brief literature review

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1381-1385

John Wiley & Sons Inc

Access to resources Recommend Favorite

A germline deletion of p14 ARF but not CDKN2A in a melanoma–neural system tumour syndrome family

By Newton Bishop J.  

Human Molecular Genetics, Vol. 10, Iss. 1, 2001-01 ,pp. : 55-62

Oxford University Press

Access to resources Recommend Favorite