A missed opportunity for preventing CMMRD: is it time to include Lynch syndrome genes in prenatal genetic testing? [PDF]
Nair G, Cadenas N, Singh A.
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Pediatric Hereditary Polyposis Syndromes: Diagnosis, Surveillance, and Management Across Evolving Guidelines. [PDF]
Khalifeh H, Zhang X, Hoskins BJ.
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Uncovering a Novel Homozygous MSH6 Variant in a Child Presenting With Glioblastoma: A Case of Constitutional Mismatch Repair Deficiency. [PDF]
Althomali A +3 more
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Bridging pediatric and adult neuro-oncology: Insights into adolescents and young adults (AYA) central nervous system tumors. [PDF]
Hennawy M +4 more
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The Tyrolean Founder <i>MLH1</i> Variant c.836T>G Causes Lynch Syndrome Due to a Leaky Splice Effect. [PDF]
Horpaopan S +12 more
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Should Sickle Cell Disease Be Considered a Cancer Predisposition Syndrome? [PDF]
Casadessus E, Pastore Y, Pincez T.
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Constitutional Mismatch Repair Deficiency, the Most Aggressive Cancer Predisposition Syndrome : Clinical Presentation, Surveillance, and Management. [PDF]
Kang E, Suh JK, Kim SD.
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Advances in the management of pediatric low-grade glioma. [PDF]
Brizini M +3 more
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Synchronous Occurrence of T-cell Lymphoblastic Lymphoma and High-Grade Glioma in a Pediatric Patient: A Case Report. [PDF]
Thakur N +4 more
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Constitutional Mismatch Repair Deficiency: Scoping Review of a Cancer-Predisposition Syndrome With Distinctive Cutaneous Findings. [PDF]
Mar K, Ameri K, Lam JM.
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