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Search Results to Mary Shago

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Shago, Mary

Item TypeName
Concept Chromosomes, Human, Pair 15
Concept Chromosomes, Human, X
Concept Chromosomes, Human, Y
Concept Chromosomes, Human, Pair 12
Concept Chromosomes, Human, Pair 17
Concept Chromosome Banding
Concept Chromosomes, Human
Concept Chromosome Breakage
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 3
Concept Chromosome Duplication
Concept Chromosomes, Human, Pair 4
Concept Chromosomes, Human, Pair 5
Concept Chromosomes, Human, Pair 21
Concept Chromosomes, Human, Pair 8
Concept Chromosome Mapping
Concept Ring Chromosomes
Concept Chromosome Aberrations
Concept Chromosome Deletion
Concept Chromosomes, Human, Pair 10
Concept Chromosomes, Human, Pair 6
Concept Chromosomes, Human, Pair 2
Concept Chromosomes, Human, Pair 13
Concept Chromosomes, Human, Pair 9
Concept Chromosomes, Artificial, Bacterial
Concept Chromosome Disorders
Concept Chromosomes, Human, Pair 22
Academic Article Cryptic insertion of MLL gene into 9p22 leads to MLL-MLLT3 (AF9) fusion in a case of acute myelogenous leukemia.
Academic Article Leptomeningeal precursor B-cell lymphoblastic lymphoma in a child with minimal bone marrow involvement.
Academic Article Occurrence of t(8;22)(q24.1;q11.2) involving the MYC locus in a case of pediatric acute lymphoblastic leukemia with a precursor B cell immunophenotype.
Academic Article Primary subcutaneous primitive neuroectodermal tumor with aggressive behavior and an unusual karyotype: case report.
Academic Article TEL-AML1 fusion in acute lymphoblastic leukemia with L3 morphology.
Academic Article Characterization of trisomy 8 in pediatric undifferentiated sarcomas using advanced molecular cytogenetic techniques.
Academic Article The diploid genome sequence of an individual human.
Academic Article Childhood acute myeloid leukemia with hemophagocytosis by the blasts and inv(8)(p11q13) with MOZ-TIF2 fusion transcripts.
Academic Article Childhood myeloid/natural killer precursor acute leukemia with novel chromosomal aberrations der(5)t(4;5)(q31;q31.3) and t(14;17)(q32;q23).
Academic Article Translocation (X;10) in a child with therapy-related acute myeloid leukemia following chemotherapy for Ewing's Sarcoma.
Academic Article Structural variation of chromosomes in autism spectrum disorder.
Academic Article Molecular breakpoint mapping of 6q11-q14 interstitial deletions in seven patients.
Academic Article Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting.
Academic Article Detailed cytogenetic and array analysis of pediatric primitive sarcomas reveals a recurrent CIC-DUX4 fusion gene event.
Academic Article 13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review.
Academic Article A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromes.
Academic Article Cockayne syndrome caused by paternally inherited 5 Mb deletion of 10q11.2 and a frameshift mutation of ERCC6.
Academic Article Cribriform neuroepithelial tumour: novel clinicopathological, ultrastructural and cytogenetic findings.
Academic Article Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndrome.
Academic Article Mosaic microdeletion of 17p11.2-p12 and duplication of 17q22-q24 in a girl with Smith-Magenis phenotype and peripheral neuropathy.
Academic Article The impact of category, cytopathology and cytogenetics on development and progression of clonal and malignant myeloid transformation in inherited bone marrow failure syndromes.
Academic Article Chromosome Preparation for Acute Lymphoblastic Leukemia.
Academic Article Recurrent Cytogenetic Abnormalities in Acute Lymphoblastic Leukemia.
Academic Article An active ring X and haploinsufficiency of SHOX contribute to short stature, congenital anomalies, and developmental delay in a female.
Academic Article Molecular testing prognostic of low risk in epithelioid uveal melanoma in a child.
Academic Article Aggressive embryonal rhabdomyosarcoma in a 3-month-old boy: A clinical and molecular analysis.
Academic Article MYCN Amplified Relapse Following Resolution of MYCN Nonamplified 4S Neuroblastoma With Placental Involvement: A Case Report and Review of the Literature.
Academic Article Masked hypodiploidy: Hypodiploid acute lymphoblastic leukemia (ALL) mimicking hyperdiploid ALL in children: A report from the Children's Oncology Group.
Academic Article Genetic diversity in alveolar soft part sarcoma: A subset contain variant fusion genes, highlighting broader molecular kinship with other MiT family tumors.
Academic Article Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemia.
Academic Article First report of t(5;11) KMT2A-MAML1 fusion in de novo infant acute lymphoblastic leukemia.
Academic Article Pediatric fibromyxoid soft tissue tumor with PLAG1 fusion: A novel entity?

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  • Chromosomes