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Publications by Colin C Pritchard
Germline ETV6 Mutations in Familial Thrombocytopenia and Hematologic Malignancy
Nature Genetics
Genetics
Polyposis Caused by Low APC Mosaicism
Journal of Genetic Syndromes & Gene Therapy
Related publications
Germline Mutations in Japanese Familial Pancreatic Cancer Patients
Oncotarget
Oncology
Lack of Germline CDK6 Mutations in Familial Melanoma
Oncogene
Cancer Research
Genetics
Molecular Biology
No Evidence of Germline PTEN Mutations in Familial Prostate Cancer
Journal of Medical Genetics
Genetics
Coexisting NRAS and BRAF Mutations in Primary Familial Melanomas With Specific CDKN2A Germline Alterations
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Acquired Somatic ATRX Mutations in Myelodysplastic Syndrome Associated With Thalassemia (ATMDS) Convey a More Severe Hematologic Phenotype Than Germline ATRX Mutations
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Two Co-Existing Germline Mutations P53 V157D and PMS2 R20Q Promote Tumorigenesis in a Familial Cancer Syndrome
Cancer Letters
Cancer Research
Oncology
Novel Germline Mutations and Unclassified Variants of BRCA1 and BRCA2 Genes in Chinese Women With Familial Breast/Ovarian Cancer
BMC Cancer
Cancer Research
Oncology
Genetics
Mutation Cluster Region, Association Between Germline and Somatic Mutations and Genotype-Phenotype Correlation in Upper Gastrointestinal Familial Adenomatous Polyposis
American Journal of Pathology
Forensic Medicine
Pathology
Respiratory Syncytial Virus in Hematopoietic Cell Transplant Recipients and Hematologic Malignancy Patients
Haematologica
Hematology
