Pages that link to "Q55468550"

The following pages link to Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations. (Q55468550):

Displaying 39 items.

• Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer (Q26797255) (← links)
• Realizing the promise of cancer predisposition genes (Q30743260) (← links)
• Monozygotic twins with Neurofibromatosis type 1, concordant phenotype and synchronous development of MPNST and metastasis (Q33650336) (← links)
• Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID (Q33678784) (← links)
• Constitutional mismatch repair deficiency and childhood leukemia/lymphoma--report on a novel biallelic MSH6 mutation (Q33829127) (← links)
• Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations (Q34160516) (← 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)
• The germline variants in DNA repair genes in pediatric medulloblastoma: a challenge for current therapeutic strategies (Q36334648) (← links)
• Mismatch repair deficiency: a temozolomide resistance factor in medulloblastoma cell lines that is uncommon in primary medulloblastoma tumours (Q36387895) (← links)
• Familial T-cell non-Hodgkin lymphoma caused by biallelic MSH2 mutations (Q37004663) (← links)
• Lessons from the skin--cutaneous features of familial cancer (Q37153048) (← links)
• Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum (Q37326213) (← links)
• Analysis of microsatellite instability in medulloblastoma (Q37395329) (← links)
• The gastrointestinal phenotype of germline biallelic mismatch repair gene mutations (Q37763509) (← links)
• The Diagnostic and Clinical Significance of Café-au-lait Macules (Q37796203) (← links)
• High‐grade brain tumors in siblings with biallelic MSH6 mutations (Q37889843) (← links)
• DNA repair: the link between primary immunodeficiency and cancer (Q37974984) (← links)
• Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD). (Q38204965) (← links)
• Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort. (Q38576104) (← links)
• Functional and physical interaction between the mismatch repair and FA-BRCA pathways (Q38755812) (← links)
• Connections between constitutional mismatch repair deficiency syndrome and neurofibromatosis type 1. (Q38806007) (← links)
• Monogenic mutations associated with IgA deficiency (Q38856255) (← links)
• Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium (Q40146955) (← links)
• Constitutional mismatch repair-deficiency syndrome (Q42793022) (← links)
• Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome (Q45400063) (← links)
• Atypical dermal melanocytosis: a diagnostic clue in constitutional mismatch repair deficiency syndrome. (Q47123439) (← links)
• Diagnostic challenges in a child with early onset desmoplastic medulloblastoma and homozygous variants in MSH2 and MSH6. (Q47231154) (← links)
• Cerebral primitive neuroectodermal tumor in an adult with a heterozygous MSH2 mutation (Q47951157) (← links)
• Constitutional or biallelic? Settling on a name for a recessively inherited cancer susceptibility syndrome. (Q48146002) (← links)
• Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I. (Q55465499) (← links)
• Genetic Counselors' Experiences Regarding Communication of Reproductive Risks with Autosomal Recessive Conditions found on Cancer Panels (Q56766232) (← links)
• Constitutional mismatch repair-deficiency: current problems and emerging therapeutic strategies (Q59128454) (← links)
• No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency. (Q64938518) (← links)
• Childhood T-cell non-Hodgkin's lymphoma, colorectal carcinoma and brain tumor in association with café-au-lait spots caused by a novel homozygous PMS2 mutation (Q79845333) (← links)
• RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference (Q79927330) (← links)
• Acute myeloid leukaemia associated with Muir‐Torre variant of hereditary non‐polyposis colon cancer (HNPCC): implications for inherited and acquired mutations in DNA mismatch repair genes (Q84938042) (← links)
• Molecular-Clinical Correlation in Pediatric Medulloblastoma: A Cohort Series Study of 52 Cases in Taiwan (Q90308673) (← links)
• LncRNA NR-104098 Inhibits AML Proliferation and Induces Differentiation Through Repressing EZH2 Transcription by Interacting With E2F1 (Q91975820) (← links)