D. Walker

发表

Large-scale discovery of novel genetic causes of developmental disorders

Tomas W. Fitzgerald, M. Hurles, J. Barrett, 2014, Nature.

Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

G. J. Swaminathan, N. Carter, M. Hurles, 2019, American journal of human genetics.

Ocular clinicopathologic study of the mitochondrial encephalomyopathy overlap syndromes.

W. Green, D. Walker, I. Maumenee, 1993, Archives of ophthalmology.

High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11.

H. Stöhr, D. Walker, C. Jones, 1994, American journal of human genetics.

Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases.

E. Zrenner, B. Wissinger, D. Walker, 1996, The British journal of ophthalmology.

CNVs affecting cancer predisposing genes (CPGs) detected as incidental findings in routine germline diagnostic chromosomal microarray (CMA) testing

J. Clayton-Smith, D. Evans, G. Hall, 2017, Journal of Medical Genetics.

Tumor Heterogeneity in a Follicular Carcinoma of Thyroid: a Study by Comparative Genomic Hybridization

A. Vargas, S. Lakhani, P. Simpson, 2011, Endocrine pathology.

Molecular evidence for non-penetrance in Best's disease.

D. Walker, B. Müller, B. Weber, 1994, Journal of medical genetics.

Best's vitelliform dystrophy (VMD2) maps between D11S903 and PYGM: no evidence for locus heterogeneity.

L. Mar, D. Walker, B. Müller, 1994, Genomics.