Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11

The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth

(2011) Sally Ann Lynch et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Structural Variation in the Human Genome and its Role in Disease

(2010) Paweł Stankiewicz et al.   Annual Review of Medicine

BAMBI (Bone Morphogenetic Protein and Activin Membrane-Bound Inhibitor) Reveals the Involvement of the Transforming Growth Factor-  Family in Pain Modulation

(2010) M. Tramullas et al.   JOURNAL OF NEUROSCIENCE

Copy Number Variation in Human Health, Disease, and Evolution

(2009) Feng Zhang et al.   Annual Review of Genomics and Human Genetics

Noncoding RNAs in mental retardation

(2009) KE Szulwach et al.   CLINICAL GENETICS

Wac: a new Augmin subunit required for chromosome alignment but not for acentrosomal microtubule assembly in female meiosis

(2009) Ana M. Meireles et al.   JOURNAL OF CELL BIOLOGY

Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects

(2009) Xavier H. Jaglin et al.   TRENDS IN GENETICS

Augmin: a protein complex required for centrosome-independent microtubule generation within the spindle

(2008) Gohta Goshima et al.   JOURNAL OF CELL BIOLOGY