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Publications by Raoul Hinze
Over-Representation of a Germline RET Sequence Variant in Patients With Sporadic Medullary Thyroid Carcinoma and Somatic RET Codon 918 Mutation
Oncogene
Cancer Research
Genetics
Molecular Biology
Significance of Proliferative Activity and DNA Ploidy in Pancreatic Cancer and Chronic Pancreatitis
International Journal of Gastrointestinal Cancer
Related publications
RET Mutation p.S891A in a Chinese Family With Familial Medullary Thyroid Carcinoma and Associated Cutaneous Amyloidosis Binding OSMR Variant p.G513D
Oncotarget
Oncology
Child With Ret Proto-Oncogene Codon 634 Mutation
Turkish Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Germline Mutation of RET Codon 883 in Two Cases of De Novo MEN 2B
Oncogene
Cancer Research
Genetics
Molecular Biology
A Founding Locus Within the RET Proto-Oncogene May Account for a Large Proportion of Apparently Sporadic Hirschsprung Disease and a Subset of Cases of Sporadic Medullary Thyroid Carcinoma
American Journal of Human Genetics
Genetics
Emergence of a RET V804M Gatekeeper Mutation During Treatment With Vandetanib in RET-Rearranged NSCLC
Journal of Thoracic Oncology
Medicine
Oncology
Respiratory Medicine
Pulmonary
Kindred With Prominent Corneal Nerves Associated With a Mutation in Codon 804 of RET on Chromosome 10q11
Archives of Ophthalmology
Novel Rearrangements Involving the RET Gene in Papillary Thyroid Carcinoma
Cancer genetics
Cancer Research
Genetics
Molecular Biology
Genetic Risk Association of CDKN1A and RET Gene SNPs With Medullary Thyroid Carcinoma: Results From the Largest MTC Cohort and Meta‐analysis
Cancer Medicine
Cancer Research
Nuclear Medicine
Radiology
Imaging
Oncology
Oncocytic Variant of Medullary Thyroid Carcinoma - A Case Report
