1. Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish family;Baehring;Am J Hum Genet,1997
2. A new case of partial monosomy of chromosome 12,del(12)(p11.01 to p12.109) confirming the location of the gene for lactate dehydrogenase B;Boilly-Dartigalongue;Ann Genet,1985
3. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes;Bucan;PLoS Genet,2009
4. Deletions of NRXN1 [Neurexin 1] predispose to a wide spectrum of developmental disorders;Ching;Am J Med Genet Part B,2010
5. Interstitial deletion of the short arm of chromosome 12;Fryns;Ann Genet,1990