Ross McLeod

Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

H.‐J. Lüdecke, Jörg Schaper, Peter Meinecke et al. · The American Journal of Human Genetics · 2001 · 234 citations · Full text

Genetic Disorder, Genetics, Genetic Epidemiology +4

A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots.

Darcy Whiteside, Ross McLeod, Gail E. Graham et al. · PubMed · 2002 · 142 citations

Multiple Café-au-lait Spots, Genetics, Pathology +16

Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta

Mathilde Huckert, Corinne Stoetzel, Supawich Morkmued et al. · Human Molecular Genetics · 2015 · 48 citations · Full text

Genetics, Pathology, Gene Cause Brachyolmia +16

Exome Sequencing Identifies a Novel Variant in ACTC1 Associated With Familial Atrial Septal Defect

Steven C. Greenway, Ross McLeod, Stacey Hume et al. · Canadian Journal of Cardiology · 2013 · 36 citations

Novel Variant, Mendelian Disorder, Genetic Disorder +9

Management of Fruit Flies in the Pacific

Ross McLeod · AgEcon Search (University of Minnesota, USA) · 2005 · 34 citations · Full text