Pages that link to "Q80513051"
Jump to navigation
Jump to search
The following pages link to A homozygous MSH6 mutation in a child with café-au-lait spots, oligodendroglioma and rectal cancer (Q80513051):
Displaying 28 items.
- A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes. (Q30252766) (← links)
- An Msh2 conditional knockout mouse for studying intestinal cancer and testing anticancer agents (Q33822488) (← links)
- Loss of the mismatch repair protein MSH6 in human glioblastomas is associated with tumor progression during temozolomide treatment (Q33865925) (← links)
- Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome (Q34326738) (← links)
- Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis (Q34350807) (← links)
- Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1. (Q34686576) (← links)
- Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg? (Q34809944) (← links)
- Somatic POLE mutations cause an ultramutated giant cell high-grade glioma subtype with better prognosis (Q36082471) (← links)
- Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations (Q36338216) (← links)
- The hMSH2(M688R) Lynch syndrome mutation may function as a dominant negative (Q36447028) (← links)
- Association of MSH6 mutation with glioma susceptibility, drug resistance and progression (Q37108779) (← links)
- Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum (Q37326213) (← links)
- The Diagnostic and Clinical Significance of Café-au-lait Macules (Q37796203) (← links)
- Diagnosing Hereditary Colorectal Cancer (Q37797761) (← links)
- High‐grade brain tumors in siblings with biallelic MSH6 mutations (Q37889843) (← links)
- Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation. (Q38301022) (← links)
- Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium (Q40146955) (← links)
- Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome (Q45400063) (← links)
- A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy (Q48582050) (← links)
- Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor (Q48684523) (← links)
- Back to the future: proceedings from the 2010 NF Conference. (Q55130390) (← links)
- Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I. (Q55465499) (← links)
- Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations. (Q55468550) (← links)
- Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies (Q55670368) (← links)
- Constitutional mismatch repair-deficiency: current problems and emerging therapeutic strategies (Q59128454) (← links)
- RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference (Q79927330) (← links)
- Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes (Q81280342) (← links)
- Pitfalls in molecular analysis for mismatch repair deficiency in a family with biallelic pms2 germline mutations (Q83123050) (← links)