Category:Pages using PMID magic links
Pages in category "Pages using PMID magic links"
The following 200 pages are in this category, out of 219 total.
(previous page) (next page)A
- ABL1
- Acinic cell carcinoma
- ACMG technical standards and guidelines: chromosome studies of lymph node and solid tumor–acquired chromosomal abnormalities (2016)
- ACMG technical standards and guidelines: microarray analysis for chromosome abnormalities in neoplastic disorders (2013)
- Acute Erythroid Leukemia
- HAEM4Backup:Acute Myeloid Leukemia (AML) and Related Precursor Neoplasms
- HAEM4:Acute Myeloid Leukemia (AML) and Related Precursor Neoplasms
- Acute Myeloid Leukemia (AML) with Mutated FLT3
- HAEM4Backup:Acute Myeloid Leukemia (AML) with t(4;12)(q12;p13); CHIC2-ETV6
- HAEM4:Acute Myeloid Leukemia (AML) with t(4;12)(q12;p13); CHIC2-ETV6
- Acute Myeloid Leukemia (AML) with UPD 13
- Adenocarcinoma
- Adenomyoepithelioma with carcinoma
- AML Table: Recurrent Genomic Alterations Detected by Chromosomal Microarray
- Anaplastic astrocytoma, IDH-mutant
- Anaplastic astrocytoma, IDH-wildtype
- Anaplastic astrocytoma, NOS
- Anaplastic ependymoma
- Anaplastic ganglioglioma
- Anaplastic oligoastrocytoma, NOS
- Anaplastic oligodendroglioma, IDH-mutant and 1p/19q-codeleted
- Anaplastic oligodendroglioma, NOS
- Anaplastic pleomorphic xanthoastrocytoma
- Angiosarcoma
- ANKRD26
- Astroblastoma
- ASXL1
- Atypical choroid plexus papilloma
- Atypical teratoid/rhabdoid tumor
B
C
- CALR
- Carcinoma of male breast
- Carcinoma with apocrine differentiation
- Carcinoma with medullary features
- Carcinoma with neuroendocrine features
- Carcinoma with signet-ring-cell differentiation
- CBFB
- CBL
- CBLB
- CEBPA
- CHIC2
- Choriocarcinoma
- Choroid plexus carcinoma
- Choroid plexus papilloma
- CLL Tables: Regions of Recurrent Copy Number Change and CN-LOH
- CNA Database
- CNS embryonal tumor with rhabdoid features
- CNS embryonal tumor, NOS
- CNS ganglioneuroblastoma
- CNS metastatic tumors
- CNS neuroblastoma
- Craniopharyngioma
- Cribriform carcinoma
- CSF3R
- CUX1
D
E
G
I
L
M
- Malignant soft tissue tumours
- Malignant tumours
- MAP2K1
- Mature teratoma
- MDS, MDS/MPN and MPN Tables: Recurrent Genomic Alterations Detected by Chromosomal Microarray
- MECOM
- Medulloblastoma with extensive nodularity
- Medulloblastoma, classic
- Medulloblastoma, histologically defined
- Medulloblastoma, non-WNT/non-SHH
- Medulloblastoma, NOS
- Medulloblastoma, SHH-activated, TP53-mutant
- Medulloblastoma, SHH-activated, TP53-wild-type
- Medulloblastomas, genetically defined
- Medulloepithelioma
- Melanoma skin Cancer
- Meningioma
- Metaplastic carcinoma
- Microglandular adenosis
- Mixed germ cell tumor
- MKL1
- MLLT3
- MPL
- Mucinous carcinoma
- MYD88
- HAEM4Backup:Myelodysplastic Syndrome (MDS) with Isolated del(5q)
- HAEM4:Myelodysplastic Syndrome (MDS) with Isolated del(5q)
- Myeloid Neoplasms with Germ Line Predisposition
- Myoepithelial carcinoma
- Myofibroblastoma
- Myxopapillary ependymoma