Five patients with novel overlapping interstitial deletions in 8q22.2q22.3

A case of 8q22.1 microdeletion without the Nablus mask-like facial syndrome phenotype

(2010) Shailly Jain et al.   European Journal of Medical Genetics

Cohen syndrome diagnosis using whole genome arrays

(2010) N. Rivera-Brugues et al.   JOURNAL OF MEDICAL GENETICS

The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature

(2009) Annick Raas-Rothschild et al.   European Journal of Medical Genetics

Deletions in theVPS13B(COH1) gene as a cause of Cohen syndrome

(2009) I. Balikova et al.   HUMAN MUTATION

Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis

(2009) L. E. L. M. Vissers et al.   JOURNAL OF MEDICAL GENETICS

Cohen syndrome resulting from a novel large intragenicCOH1deletion segregating in an isolated Greek island population

(2008) Marianna Bugiani et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Novel microdeletion syndromes detected by chromosome microarrays

(2008) Anne M. Slavotinek   HUMAN GENETICS