Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes

Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes

Item
http://www.wikidata.org/entity/Q34400180
Array CGH in human leukemia: from somatics to genetics.Identification of clinically important chromosomal aberrations in acute myeloid leukemia by array-based comparative genomic hybridization.Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cellsIdentification of novel genomic aberrations in AML-M5 in a level of array CGHDerivation of normal diploid human embryonic stem cells from tripronuclear zygotes with analysis of their copy number variation and loss of heterozygosity.Genomic Copy Number Variations in the Myelodysplastic Syndrome and Acute Myeloid Leukemia Patients with del(5q) and/or -7/del(7q).Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes.Relapse after Allogeneic Hematopoietic Cell Transplantation for Myelodysplastic Syndromes: Analysis of Late Relapse Using Comparative Karyotype and Chromosome Genome Array TestingUpdates in cytogenetics and molecular markers in MDS.The need for additional genetic markers for myelodysplastic syndrome stratification: what does the future hold for prognostication?Chromosome dynamic changes in two cultured Chinese human embryonic stem cell lines: single nucleotide polymorphism, copy number variation and loss of heterozygosity.An interstitial 20q11.21 microdeletion causing mild intellectual disability and facial dysmorphisms.Techniques for detecting chromosomal aberrations in myelodysplastic syndromesDifferent loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms.Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemiaMyelodysplastic syndromes: advantages of a combined cytogenetic and molecular diagnostic workup.Impact of copy neutral loss of heterozygosity and total genome aberrations on survival in myelodysplastic syndrome.
P2860

Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes

Item
http://www.wikidata.org/entity/Q34400180
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Assessing karyotype precision ...... c/myeloproliferative syndromes
@ast
Assessing karyotype precision ...... c/myeloproliferative syndromes
@en
Assessing karyotype precision ...... c/myeloproliferative syndromes
@nl
type
label
Assessing karyotype precision ...... c/myeloproliferative syndromes
@ast
Assessing karyotype precision ...... c/myeloproliferative syndromes
@en
Assessing karyotype precision ...... c/myeloproliferative syndromes
@nl
prefLabel
Assessing karyotype precision ...... c/myeloproliferative syndromes
@ast
Assessing karyotype precision ...... c/myeloproliferative syndromes
@en
Assessing karyotype precision ...... c/myeloproliferative syndromes
@nl
P1433
P1476
P2093
P2860
P2888
P304
P31
P356
P478
P50
P577
P5875
P6179
P698
P921
P932
P356
P1433
P1476
Assessing karyotype precision ...... c/myeloproliferative syndromes
@en
P2093
P2860
P2888
P304
P31
P356
P478
P50
P577
P5875
P6179
P698
P921
P932