Delineation of 2q32q35 Deletion Phenotypes: Two Apparent “Proximal” and “Distal” Syndromes

Por Mc Cormack, Adrian, Taylor, Juliet, Gregersen, Nerine, George, Alice M., Love, Donald R.
Publicado em 2013

A Case of 17q21.31 Microduplication and 7q31.33 Microdeletion, Associated with Developmental Delay, Microcephaly, and Mild Dysmorphic Features

Por Mc Cormack, Adrian, Taylor, Juliet, Te Weehi, Leah, Love, Donald R., George, Alice M.
Publicado em 2014

12q14 Microdeletions: Additional Case Series with Confirmation of a Macrocephaly Region

Por Mc Cormack, Adrian, Sharpe, Cynthia, Gregersen, Nerine, Smith, Warwick, Hayes, Ian, George, Alice M., Love, Donald R.
Publicado no Case Rep Genet (2015)

Microduplication of 3p26.3 Implicated in Cognitive Development

Por Te Weehi, Leah, Maikoo, Raj, Mc Cormack, Adrian, Mazzaschi, Roberto, Ashton, Fern, Zhang, Liangtao, George, Alice M., Love, Donald R.
Publicado em 2014

Microarray testing in clinical diagnosis: an analysis of 5,300 New Zealand patients

Por Mc Cormack, Adrian, Claxton, Karen, Ashton, Fern, Asquith, Philip, Atack, Edward, Mazzaschi, Roberto, Moverley, Paula, O’Connor, Rachel, Qorri, Methat, Sheath, Karen, Love, Donald R., George, Alice M.
Publicado no Mol Cytogenet (2016)