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Giant marker chromosomes in cancer
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创建时间：
2017-12-22
相关数据集
Reads pairs with discordant reads mapping to 7p15 and 7q21 within 200 bp of each other.
Reads pairs with discordant reads mapping to 7p15 and 7q21 within 200 bp of each other.
Figshare2016-06-09 更新30
Additional file 1 of Chromosome 17p13 deletion is associated with an aggressive tumor phenotype in clear cell renal cell carcinoma
Additional file 1: Table S1. Pathological and clinical data of the arrayed renal cell tumors.
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Refinement of 1p36 Alterations Not Involving PRDM16 in Myeloid and Lymphoid Malignancies
Fluorescence in situ hybridization was performed to characterize 81 cases of myeloid and lymphoid malignancies with cytogenetic 1p36 alterations not affecting the PRDM16 locus. In total, three subgrou
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The MLH1 c.-27C>A and c.85G>T variants are borne on a European ancestral haplotype which underlies an autosomal dominant form of MLH1 epimutation.
Lynch syndrome, caused by germline heterozygous mutations of the DNA mismatch repair genes MLH1, MSH2, MSH6 and PMS2, or deletions affecting the EPCAM gene upstream of MSH2, is characterized by a pred
NIAID Data Ecosystem30
PROFIL GENETIQUE DES LEUCEMIES AIGUES LYMPHOBLASTIQUES AU SERVICE DHEMATOLOGIE ET DONCOLOGIE PEDIATRIQUE DE MARRAKECH : A PROPOS DE 49 CAS
Les leucemies aigues (LA) constituent un groupe dhemopathies malignes caracterise par une proliferation monoclonale intra-medullaire de cellules hematopoietiques anormales dont le processus de maturat
NIAID Data Ecosystem20
