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Publications by Pat Concannon
Fine Localization of the Nijmegen Breakage Syndrome Gene to 8q21: Evidence for a Common Founder Haplotype
American Journal of Human Genetics
Genetics
An Unusual Mutation in RECQ4 Gene Leading to Rothmund–Thomson Syndrome
Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
Mutagenesis
Toxicology
Health
Molecular Biology
Genetics
Related publications
Mutations in the Nijmegen Breakage Syndrome Gene in Medulloblastomas
Clinical Cancer Research
Cancer Research
Oncology
Nijmegen Breakage Syndrome-Like Disorder
Genetic Mapping Using Microcell-Mediated Chromosome Transfer Suggests a Locus for Nijmegen Breakage Syndrome at Chromosome 8q21-24
American Journal of Human Genetics
Genetics
Nijmegen Breakage Syndrome Gene, NBS1, and Molecular Links to Factors for Genome Stability
Oncogene
Cancer Research
Genetics
Molecular Biology
Heterozygous Carriers of Nijmegen Breakage Syndrome Have a Distinct Gene Expression Phenotype
Genome Research
Genetics
Haploinsufficiency of the Nijmegen Breakage Syndrome 1 Gene Increases Mammary Tumor Latency and Metastasis
International Journal of Oncology
Cancer Research
Oncology
Inactivation of the Nijmegen Breakage Syndrome Gene Leads to Excess Centrosome Duplication via the ATR/BRCA1 Pathway
Cancer Research
Cancer Research
Oncology
Evidence for a Pre-Malignant Cell Line in a Skin Biopsy From a Patient With Nijmegen Breakage Syndrome
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Human RAD50 Deficiency in a Nijmegen Breakage Syndrome-Like Disorder
American Journal of Human Genetics
Genetics
