UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 59

Sortiert nach

Balanced complex chromosome rearrangement in male infertility: case report and literature review

Andrologia, 2015-03, Vol.47 (2), p.178-185

2015

Volltextzugriff (PDF)

Aneuploidy and DNA Fragmentation in Sperm of Carriers of a Constitutional Chromosomal Abnormality

Cytogenetic and genome research, 2011-04, Vol.133 (2-4), p.100-106

2011

Volltextzugriff (PDF)

Fluorescence in situ hybridization characterization of ider(20q) in myelodysplastic syndrome

British journal of haematology, 2008-12, Vol.143 (5), p.716-720

2008

Volltextzugriff (PDF)

Molecular characterization of deletions of the long arm of chromosome 5 (del(5q)) in 94 MDS/AML patients

Leukemia, 2012-07, Vol.26 (7), p.1695-1697

2012

Volltextzugriff (PDF)

236 Molecular characterization of deletion of the long arm of chromosome 5 (del5q) in 86 MDS/AML patients

Leukemia research, 2011, Vol.35, p.S93-S93

2011

Volltextzugriff (PDF)

Isoderivative of deleted chromosome 20 in primary myelofibrosis (PMF) characterized by molecular cytogenetics and array CGH

Annals of hematology, 2009-11, Vol.88 (11), p.1157-1159

2009

Volltextzugriff (PDF)

Gene Expression Profiling of Adult t(4;11)(q21;q23)-associated Acute Lymphoblastic Leukemia Reveals a Different Signature from Pediatric Cases

Anticancer research, 2012-09, Vol.32 (9), p.3893-3899

2012

Volltextzugriff (PDF)

Double Inv(3)(q21q26), a rare but recurrent chromosomal abnormality in myeloid hemopathies

Anticancer research, 2013-02, Vol.33 (2), p.639-642

2013

Volltextzugriff (PDF)

Stratégies d’identification des marqueurs chromosomiques surnuméraires en cytogénétique constitutionnelle

Pathologie biologie (Paris), 2008-09, Vol.56 (6), p.362-367

2008

Volltextzugriff (PDF)

Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics

Pathologie biologie (Paris), 2008-09, Vol.56 (6), p.362-367

2008

Volltextzugriff (PDF)

Stratégies d'identification des marqueurs chromosomiques surnuméraires en cytogénétique constitutionnelle: Génétique

Pathologie biologie (Paris), 2008, Vol.56 (6), p.362-367

2008

Volltextzugriff (PDF)

Isoderivative of deleted chromosome 20 in primary myelofibrosis (PMF) characterized by molecular cytogenetics and array CGH

Annals of hematology, 2009, Vol.88 (11), p.1157-1159

2009

Volltextzugriff (PDF)

Asian Population Is More Prone to Develop High-Risk Myelodysplastic Syndrome, Concordantly with Their Propensity to Exhibit High-Risk Cytogenetic Aberrations

Cancers, 2021-01, Vol.13 (3), p.481

2021

Volltextzugriff (PDF)

ETV6 fusion genes in hematological malignancies: A review

Leukemia research, 2012-08, Vol.36 (8), p.945-961

2012

Volltextzugriff (PDF)

A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.844-851

2016

Volltextzugriff (PDF)

3q26/EVI1 rearrangements in myeloid hemopathies: a cytogenetic review

Future oncology (London, England), 2015-06, Vol.11 (11), p.1675-1686

2015

Volltextzugriff (PDF)

Hox gene dysregulation in acute myeloid leukemia

Future oncology (London, England), 2014-02, Vol.10 (3), p.475-495

2014

Volltextzugriff (PDF)

Acute myeloid leukaemia (FAB AML‐M4Eo) with cryptic insertion of cbfb resulting in cbfb‐Myh11 fusion

Hematological oncology, 2017-09, Vol.35 (3), p.385-389

2017

Volltextzugriff (PDF)

Translocations involving 13q14 without associated deletion in chronic lymphoid leukaemia target DLEU2

British journal of haematology, 2016-02, Vol.172 (3), p.467-469

2016

Volltextzugriff (PDF)

Immunoglobulin gene translocations in chronic lymphocytic leukemia: A report of 35 patients and review of the literature

Molecular and clinical oncology, 2016-05, Vol.4 (5), p.682-694

2016

Volltextzugriff (PDF)

Recurrent translocation (10;17)(p15;q21) in acute poorly differentiated myeloid leukemia likely results in ZMYND11-MBTD1 fusion

Leukemia & lymphoma, 2014-05, Vol.55 (5), p.1189-1190

2014

Volltextzugriff (PDF)

Acute myeloid leukaemia (FAB AML-M4Eo) with cryptic insertion of cbfb resulting in cbfb-Myh11 fusion: Cryptic ins(16) in AML

Hematological oncology, 2017-09, Vol.35 (3), p.385-389

2017

Volltextzugriff (PDF)

Breakpoint heterogeneity in (2;3)(p15–23;q26) translocations involving EVI1 in myeloid hemopathies

Blood cells, molecules, & diseases, 2015-02, Vol.54 (2), p.160-163

2015

Volltextzugriff (PDF)

Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions

Annals of hematology, 2008-07, Vol.87 (7), p.537-544

2008

Volltextzugriff (PDF)

3q26

Future oncology (London, England), 2015-06, Vol.11 (11), p.1675-1686

2015

Volltextzugriff (PDF)

1 – 25 von 59

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(46)
Mit Volltextzugriff
(44)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(38)
Life Sciences & Biomedicine
(37)
Science & Technology
(37)
Female
(24)
Oncology
(22)
Male
(21)
In Situ Hybridization, Fluorescence
(18)
Hematology
(16)
Translocation, Genetic
(15)
Adult
(12)
Aged
(12)
Middle Aged
(12)
Genetics & Heredity
(10)
Karyotyping
(10)
Biological And Medical Sciences
(9)
Leukemia, Myeloid, Acute - Genetics
(9)
Medical Sciences
(9)
Chromosome Aberrations
(7)
Chromosome Deletion
(7)
Cytogenetics
(7)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Balanced complex chromosome rearrangement in male infertility: case report and literature review

Aneuploidy and DNA Fragmentation in Sperm of Carriers of a Constitutional Chromosomal Abnormality

Fluorescence in situ hybridization characterization of ider(20q) in myelodysplastic syndrome

Molecular characterization of deletions of the long arm of chromosome 5 (del(5q)) in 94 MDS/AML patients

236 Molecular characterization of deletion of the long arm of chromosome 5 (del5q) in 86 MDS/AML patients

Isoderivative of deleted chromosome 20 in primary myelofibrosis (PMF) characterized by molecular cytogenetics and array CGH

Gene Expression Profiling of Adult t(4;11)(q21;q23)-associated Acute Lymphoblastic Leukemia Reveals a Different Signature from Pediatric Cases

Double Inv(3)(q21q26), a rare but recurrent chromosomal abnormality in myeloid hemopathies

Stratégies d’identification des marqueurs chromosomiques surnuméraires en cytogénétique constitutionnelle

Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics

Stratégies d'identification des marqueurs chromosomiques surnuméraires en cytogénétique constitutionnelle: Génétique

Isoderivative of deleted chromosome 20 in primary myelofibrosis (PMF) characterized by molecular cytogenetics and array CGH

Asian Population Is More Prone to Develop High-Risk Myelodysplastic Syndrome, Concordantly with Their Propensity to Exhibit High-Risk Cytogenetic Aberrations

ETV6 fusion genes in hematological malignancies: A review

A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH

3q26/EVI1 rearrangements in myeloid hemopathies: a cytogenetic review

Hox gene dysregulation in acute myeloid leukemia

Acute myeloid leukaemia (FAB AML‐M4Eo) with cryptic insertion of cbfb resulting in cbfb‐Myh11 fusion

Translocations involving 13q14 without associated deletion in chronic lymphoid leukaemia target DLEU2

Immunoglobulin gene translocations in chronic lymphocytic leukemia: A report of 35 patients and review of the literature

Recurrent translocation (10;17)(p15;q21) in acute poorly differentiated myeloid leukemia likely results in ZMYND11-MBTD1 fusion

Acute myeloid leukaemia (FAB AML-M4Eo) with cryptic insertion of cbfb resulting in cbfb-Myh11 fusion: Cryptic ins(16) in AML

Breakpoint heterogeneity in (2;3)(p15–23;q26) translocations involving EVI1 in myeloid hemopathies

Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions

3q26

Suchergebnisse filtern