C. Boyd

Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis

L. Kluwe, S. Plotkin, M. Maccollin, 2008, Clinical genetics.

Identity analysis of schwannomatosis kindreds with recurrent constitutional SMARCB1 (INI1) alterations

S. Plotkin, M. Maccollin, M. Smith, 2009, Clinical genetics.

Blot hybridisation analysis of genomic DNA.

C. Mathew, I. Wiid, A. Bester, 1984, Journal of medical genetics.

genes in health • genetIcs human a molecular South African and disease ­ approach

C. Mathew, P. Beighton, C. Boyd, 1984 .

Mutations linked to the pro alpha 2(I) collagen gene are responsible for several cases of osteogenesis imperfecta type I.

C. Mathew, P. Beighton, C. Boyd, 1986, Journal of medical genetics.

Polymorphism of DNA sequence in the human pro alpha 2(I) collagen gene.

C. Mathew, R. Dalgleish, R. Kaufman, 1985, Journal of medical genetics.

South African human genes in health and disease--a molecular genetics approach.

C. Mathew, P. Beighton, C. Boyd, 1984, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.