Ralf Krahe, Ph.D., Molecular Geneticist

Ralf Krahe, Ph.D., Department of Genetics, Division of VP, Research

Speakers

Sydney Moyer - Postdoctoral Researcher - Dana-Farber Cancer Institute

PDF) Bi-allelic CCDC47 Variants Cause a Disorder Characterized by Woolly Hair, Liver Dysfunction, Dysmorphic Features, and Global Developmental Delay

GSBS alumni play key role on school's DEI committee - MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences

Genome‐wide loss of heterozygosity analysis of WT1–wild‐type and WT1‐mutant Wilms tumors - Ruteshouser - 2005 - Genes, Chromosomes and Cancer - Wiley Online Library

Osteoblast-Specific Overexpression of Nucleolar Protein NO66/RIOX1 in Mouse Embryos Leads to Osteoporosis in Adult Mice

Genome‐wide loss of heterozygosity analysis of WT1–wild‐type and WT1‐mutant Wilms tumors - Ruteshouser - 2005 - Genes, Chromosomes and Cancer - Wiley Online Library

MD Anderson Annual Report 2007-2008 by MD Anderson Cancer Center - Issuu

PDF) Prevalence of myotonic dystrophy in Israeli Jewish communities: Inter-community variation and founder premutations

Ralf Krahe - Professor - University of Texas MD Anderson Cancer Center

PDF) Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromes

Mario GOMES-PEREIRA, Research Associate / Chargé de Recherche, Ph.D., French Institute of Health and Medical Research, Inserm, Unit of Genetics and Epigenetics of Neurometabolic Diseases and Birth Defects

Ralf KRAHE, Professor, BS, PhD, University of Texas MD Anderson Cancer Center, Texas, MD Anderson, Department of Genetics