Ophthalmologic abnormalities in a de novo terminal 6q deletion

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

(2009) Helen V. Firth et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Fine-mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals

(2008) Cheryl DeScipio et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1–p23.1, 4q21.21–q22.1, 6q26–q27, and 21q2

(2008) William B. Dobyns et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Clinical Utility of Array CGH for the Detection of Chromosomal Imbalances Associated with Mental Retardation and Multiple Congenital Anomalies

(2008) Lisa Edelmann et al.   Annals of the New York Academy of Sciences

PGMapper: a web-based tool linking phenotype to genes

(2008) Q. Xiong et al.   BIOINFORMATICS

Terminal Deletion of Chromosome 6q

(2008) Pen-Hua Su et al.   Pediatrics and Neonatology