D. Silva

发表

Service Breast Screening Programme (NHSBSP)

F. Gilbert, N. Haites, G. Needham, 2022 .

Lanka . diabetic patients in Sri lipid abnormalities amongst macrovascular disease and The prevalence of

S. Siribaddana, S. Fernando, D. Silva, 2008 .

Genotype–Phenotype Correlations Emerging from the Identification of Missense Mutations in MBTPS2

K. Grzeschik, A. Mégarbané, R. Happle, 2013, Human mutation.

Aberdeen Genetic Clinic

N. Haites, A. Schofield, H. Gregory, 2004 .

Noncoding copy-number variations are associated with congenital limb malformation

D. Horn, S. Mundlos, M. Spielmann, 2017, Genetics in Medicine.

How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum

W. Reardon, A. Collins, J. Clayton-Smith, 2011, European Journal of Human Genetics.

rare cause of recurrent

A. Seaton, J. Dean, D. Silva, 1998 .

Medicine in the elderly Creutzfeldt-Jakob disease in the elderly

Jones, R. Knight, C. Findlay, 2003 .

Male breast cancer: the importance of recognizing family history and the preliminary results of linkage analysis to BRCA1 and BRCA2

N. Haites, A. Schofield, H. Gregory, 1996 .

Evaluation of an in house genetic testing method for confirmation of Prader - Willi and Angelman syndromes in Sri Lanka

N. Chandrasekharan, P. Rathnayake, N. Atapattu, 2021 .

A Scottish family with Bazex-Dupré-Christol syndrome: follicular atrophoderma, congenital hypotrichosis, and basal cell carcinoma.

N. Haites, J. Dean, A. Kidd, 1996, Journal of medical genetics.

Evaluation of consonant development following cleft palate surgery: Comparison of Isolated Cleft Palate Versus Pierre Robin sequence

D. Silva, R. Gunasekera, Malka Jayathilake, 2023, International Journal of Scientific and Research Publications (IJSRP).

Ascertainment of familial ovarian cancer in the Aberdeen Genetic Clinic.

N. Haites, A. Schofield, D. de Silva, 1996, Journal of medical genetics.