Ann C. M. Smith

Auditory Phenotype of Smith-Magenis Syndrome.

C. Brewer, B. Finucane, C. Zalewski, 2017, Journal of speech, language, and hearing research : JSLHR.

Co-existent pseudoxanthoma elasticum and vitamin K-dependent coagulation factor deficiency: compound heterozygosity for mutations in the GGCX gene.

J. Uitto, L. Schurgers, M. Tsokos, 2009, The American journal of pathology.

A diagnosis of Birt–Hogg–Dubé syndrome in individuals with Smith–Magenis syndrome: Recommendation for cancer screening

C. Vocke, W. Linehan, Leah Fleming, 2022, American journal of medical genetics. Part A.

Craniofacial and dental phenotype of Smith–Magenis syndrome

T. Hart, Ann C M Smith, J. Guadagnini, 2006, American journal of medical genetics. Part A.

Discriminating power of localized three-dimensional facial morphology.

A. Karmiloff-Smith, B. Buxton, P. Scambler, 2005, American journal of human genetics.

Molecular Analysis of the Retinoic Acid Induced 1 Gene (RAI1) in Patients with Suspected Smith-Magenis Syndrome without the 17p11.2 Deletion

W. Gahl, M. Huizing, T. Vilboux, 2011, PloS one.

A complete set of human telomeric probes and their clinical application

D. Ledbetter, R. Regan, J. Flint, 1996, Nature Genetics.