H. Wilson

发表

Interstitial 22q13 deletions: genes other than SHANK3 have major effects on cognitive and language development

Shuwen Huang, V. Maloney, J. Crolla, 2008, European Journal of Human Genetics.

Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms

H. McDermid, A. Wong, M. C. Phelan, 2003, Journal of medical genetics.

Unusual dicentric chromosome 22 associated with a 22q13 deletion

H. McDermid, V. D. Der Kaloustian, B. Chodirker, 2006, American journal of medical genetics. Part A.

Apparent Smith-Lemli-Opitz syndrome and Miller-Dieker syndrome in a family with segregating translocation t(7;17)(q34;p13.1).

R. Berry, R. Porreco, D. Manchester, 1989, American journal of medical genetics.