S. Ladd

Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability.

J. Lilien, A. Srivastava, G. Guzauskas, 2008, American journal of human genetics.

Identification of ectodysplasin-A receptor gene deletion at 2q12.2 and a potential autosomal MR locus

A. Srivastava, B. Dupont, A. Asamoah, 2009, European Journal of Human Genetics.

Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature

A. Srivastava, Lynn Dukes-Rimsky, Anand K. Srivastava, 2011, American journal of medical genetics. Part A.

Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism

Rebekah K. Stevenson, R. Stevenson, C. Schwartz, 2007, Clinical genetics.

Intellectual disability, midface hypoplasia, facial hypotonia, and alport syndrome are associated with a deletion in Xq22.3

R. Stevenson, C. Schwartz, N. Leslie, 2010, American journal of medical genetics. Part A.

AGTR2 Mutations in X-Linked Mental Retardation

R. Stevenson, C. Schwartz, A. Srivastava, 2002, Science.

Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies

R. Stevenson, C. Schwartz, A. Srivastava, 2005, Cytogenetic and Genome Research.

Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities.

R. Saul, A. Srivastava, B. Dupont, 2008, Genomics.

AGTR2 Mutations in X-Linked Mental Retardation

R. Stevenson, C. Schwartz, B. Dupont, 2002, Science.