J. A. Scott

Deletion 22q11: a newly recognized cause of behavioral and psychiatric disorders.

S. McCandless, N. Robin, J. A. Scott, 1998, Archives of pediatrics & adolescent medicine.

General case of the day. Moyamoya syndrome in a child with sickle cell disease.

J. A. Scott, J. Drew, G. Chua, 1993, Radiographics : a review publication of the Radiological Society of North America, Inc.

Treatment of dural sinus thrombosis with local urokinase infusion. Case report.

G. Becker, R. Pascuzzi, P. Hall, 1988, Journal of neurosurgery.

Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation.

A. Chakravarti, J. A. Scott, M. Steele, 1995, American journal of medical genetics.

Management of superior mesenteric venous thrombus in cystic fibrosis related liver disease.

V. Athwal, A. Jones, P. Barry, 2020, Paediatric respiratory reviews.

Co-occurrence of schizophrenia and Treacher Collins syndrome.

A. Chakravarti, R. Ganguli, J. Brar, 1993, American journal of medical genetics.

Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagen.

M. Warman, N. Robin, M. A. Lavery, 1998, The Journal of pediatrics.

Nonpenetrance in FGFR3-associated coronal synostosis syndrome.

N. Robin, A. Cohen, J. Goldstein, 1998, American journal of medical genetics.

Favorable prognosis for children with Pfeiffer syndrome types 2 and 3: implications for classification.

M. Cohen, N. Robin, J. Goldstein, 1998, American journal of medical genetics.