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Quoted phrase not found in phrase index: "Diaphyseal medullary stenosis-bone malignancy syndrome"
Page 1
Imaging features and differential diagnosis of multiple diaphyseal sclerosis: A case report and review of literature.
Cai Y, Lin H, Huang F, Zheng X, Huang Y, Zhang S. Cai Y, et al. Medicine (Baltimore). 2018 Aug;97(33):e11725. doi: 10.1097/MD.0000000000011725. Medicine (Baltimore). 2018. PMID: 30113457 Free PMC article. Review.
DIAGNOSES: MDS is characterized radiographically by a fusiform widening of the diaphyseal portion of the long bones, which is caused by a thickening of the cortex with obstruction of the medullary cavity. The pathologies are observed utilizing diagnostic imag …
DIAGNOSES: MDS is characterized radiographically by a fusiform widening of the diaphyseal portion of the long bones, which is caused …
Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22.
Martignetti JA, Desnick RJ, Aliprandis E, Norton KI, Hardcastle P, Nade S, Gelb BD. Martignetti JA, et al. Am J Hum Genet. 1999 Mar;64(3):801-7. doi: 10.1086/302297. Am J Hum Genet. 1999. PMID: 10053015 Free PMC article.
Diaphyseal medullary stenosis with malignant fibrous histiocytoma (DMS-MFH) is an autosomal dominant bone dysplasia/cancer syndrome of unknown etiology. ...Notably, 35% of individuals with DMS develop MFH, a highly malignant bone sarcoma. A geno …
Diaphyseal medullary stenosis with malignant fibrous histiocytoma (DMS-MFH) is an autosomal dominant bone dysplasia/can …
Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndrome.
Watts GD, Mehta SG, Zhao C, Ramdeen S, Hamilton SJ, Novack DV, Mumm S, Whyte MP, Mc Gillivray B, Kimonis VE. Watts GD, et al. Hum Genet. 2005 Dec;118(3-4):508-14. doi: 10.1007/s00439-005-0075-z. Epub 2005 Oct 22. Hum Genet. 2005. PMID: 16244874
A genome-wide scan for the disease locus obtained a maximal LOD score of 3.74 for marker GATA87E02 N (D9S1121). Haplotype analysis localized the disease gene within a 15 Mb interval flanked by markers AGAT142P and GATA5E06P. This region also localizes diaphyseal …
A genome-wide scan for the disease locus obtained a maximal LOD score of 3.74 for marker GATA87E02 N (D9S1121). Haplotype analysis lo …