21278390: High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia (Journal of Medical Genetics, 2011) Post date January 28, 2011 ← 21215367: Massive genomic rearrangement acquired in a single catastrophic event during cancer development (Cell, 2011) → 21523828: Exclusion of the GNAS locus in PHP-Ib patients with broad GNAS methylation changes: evidence for an autosomal recessive form of PHP-Ib? (Journal of Bone and Mineral Research, 2011)
