UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Rare coinheritance of hemoglobin vancleave with severe beta-thalassemia mutation in a patient with secondary erythrocytosis

Human genome variation, 2024-04, Vol.11 (1), p.19-19, Article 19

2024

Volltextzugriff (PDF)

Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries

Journal of personalized medicine, 2022-03, Vol.12 (4), p.552

2022

Volltextzugriff (PDF)

Global Globin Network and adopting genomic variant database requirements for thalassemia

Database : the journal of biological databases and curation, 2024-09, Vol.2024

2024

Volltextzugriff (PDF)

The Characteristics of Compound Heterozygosity for Hemoglobin G-Makassar with Hb E in Malaysia

Journal of blood medicine, 2024-06, Vol.15, p.255-264

2024

Volltextzugriff (PDF)

Comparison of neutrophil respiratory oxidative burst activity between flow cytometry using dihydrorhodamine (DHR) 123 and conventional nitroblue tetrazolium test (NBT)

Bangladesh journal of medical science (Ibn Sina Trust), 2022-07, Vol.21 (3), p.626-633

2022

Volltextzugriff (PDF)

An insight of -50 (G>A) mutation in the direct repeat element of the β-globin gene: From Malaysian perspective

Malaysian journal of pathology, 2022-08, Vol.44 (2), p.301-302

2022

Volltextzugriff (PDF)

Characterization of New Alpha Zero (α 0 ) Thalassaemia Deletion (-- GB ) among Malays in Malaysian Population

Diagnostics (Basel), 2023-10, Vol.13 (20), p.3286

2023

Volltextzugriff (PDF)

Clinical and haematological characteristics of 38 individuals with Hb G-Makassar in Malaysia

EJHaem, 2023-11, Vol.4 (4), p.940-948

2023

Volltextzugriff (PDF)

Molecular and hematological studies in a cohort of beta zero South East Asia deletion (β°-thal SEA) from Malaysian perspective

Frontiers in pediatrics, 2022-11, Vol.10, p.974496-974496

2022

Volltextzugriff (PDF)

Family study of haemoglobin Arya in a Malaysian family

Malaysian journal of pathology, 2024-08, Vol.46 (2), p.315-320

2024

Volltextzugriff (PDF)

Characterization of New Alpha Zero among Malays in Malaysian Population

Diagnostics (Basel), 2023-10, Vol.13 (20)

2023

Volltextzugriff (PDF)

Coinheritance of δ-Thalassemia and a Heterozygous Xmn I Polymorphism Mask the Diagnosis of Borderline Hb A 2 β-Thalassemia: A Diagnostic Challenge

Hemoglobin, 2019-11, Vol.43 (6), p.347-347

2019

Volltextzugriff (PDF)

An Insight on Beta Zero (β0) Southeast Asian Deletion (βSEA); Is it a β0-Thalassemia or Hereditary Persistence of Fetal Hemoglobin (HPFH)

Hemoglobin, 2019-11, Vol.43 (6), p.362-362

2019

Volltextzugriff (PDF)

Coinheritance of δ-Thalassemia and a Heterozygous XmnI Polymorphism Mask the Diagnosis of Borderline Hb A2 β-Thalassemia: A Diagnostic Challenge

Hemoglobin, 2019-11, Vol.43 (6), p.347-347

2019

Volltextzugriff (PDF)

An Insight on Beta Zero (β 0 ) Southeast Asian Deletion (β SEA ); Is it a β 0 -Thalassemia or Hereditary Persistence of Fetal Hemoglobin (HPFH)

Hemoglobin, 2019-11, Vol.43 (6), p.362-362

2019

Volltextzugriff (PDF)

Discovery of New Deletional α-Thalassemia Mutations Detected by Multiplex Ligation-Dependent Probe Amplification

Hemoglobin, 2019-11, Vol.43 (6), p.341-341

2019

Volltextzugriff (PDF)

β-Thalassemia Intermedia Due to Coinheritance of Three Unique α-Globin Cluster Duplications

Hemoglobin, 2019-11, Vol.43 (6), p.336-336

2019

Volltextzugriff (PDF)

"A Rare Interactions Between Heterozygous --SEA Deletion and Hb Ube-2 [α68 (E17) Asn →Asp]; First Reported Case from Malaysia"

Biomedical Journal of Scientific & Technical Research, 2023-07, Vol.51 (4)

Yasin, Norafiza Mohd

2023

Volltextzugriff (PDF)

Identification of a Novel α-Thalassemia Deletion: -(α)4.9 from a Current Multiplex Gap-Polymerase Chain Reaction

Hemoglobin, 2019-11, Vol.43 (6), p.346-346

2019

Volltextzugriff (PDF)

The Characteristics of Compound Heterozygosity for Hemoglobin G-Makassar with Hb E in Malaysia

Journal of blood medicine, 2024, Vol.15, p.255-264

2024

Volltextzugriff (PDF)

A rare case of compound heterozygous Southeast Asian double α-globin gene deletion and Haemoglobin Quong Sze in a Malay proband

Malaysian journal of pathology, 2024-08, Vol.46 (2), p.321-324

2024

Volltextzugriff (PDF)

1 – 22 von 22

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(19)
Mit Volltextzugriff
(12)

Publikationsform

Artikel
(21)
Berichte
(1)

Sprache

Englisch
(22)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Rare coinheritance of hemoglobin vancleave with severe beta-thalassemia mutation in a patient with secondary erythrocytosis

Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries

Global Globin Network and adopting genomic variant database requirements for thalassemia

The Characteristics of Compound Heterozygosity for Hemoglobin G-Makassar with Hb E in Malaysia

Comparison of neutrophil respiratory oxidative burst activity between flow cytometry using dihydrorhodamine (DHR) 123 and conventional nitroblue tetrazolium test (NBT)

Evaluation of in silico predictors on short nucleotide variants in HBA1 , HBA2 , and HBB associated with haemoglobinopathies

An insight of -50 (G>A) mutation in the direct repeat element of the β-globin gene: From Malaysian perspective

Characterization of New Alpha Zero (α 0 ) Thalassaemia Deletion (-- GB ) among Malays in Malaysian Population

Clinical and haematological characteristics of 38 individuals with Hb G-Makassar in Malaysia

Molecular and hematological studies in a cohort of beta zero South East Asia deletion (β°-thal SEA) from Malaysian perspective

Family study of haemoglobin Arya in a Malaysian family

Characterization of New Alpha Zero among Malays in Malaysian Population

Coinheritance of δ-Thalassemia and a Heterozygous Xmn I Polymorphism Mask the Diagnosis of Borderline Hb A 2 β-Thalassemia: A Diagnostic Challenge

An Insight on Beta Zero (β0) Southeast Asian Deletion (βSEA); Is it a β0-Thalassemia or Hereditary Persistence of Fetal Hemoglobin (HPFH)

Coinheritance of δ-Thalassemia and a Heterozygous XmnI Polymorphism Mask the Diagnosis of Borderline Hb A2 β-Thalassemia: A Diagnostic Challenge

An Insight on Beta Zero (β 0 ) Southeast Asian Deletion (β SEA ); Is it a β 0 -Thalassemia or Hereditary Persistence of Fetal Hemoglobin (HPFH)

Discovery of New Deletional α-Thalassemia Mutations Detected by Multiplex Ligation-Dependent Probe Amplification

β-Thalassemia Intermedia Due to Coinheritance of Three Unique α-Globin Cluster Duplications

"A Rare Interactions Between Heterozygous --SEA Deletion and Hb Ube-2 [α68 (E17) Asn →Asp]; First Reported Case from Malaysia"

Identification of a Novel α-Thalassemia Deletion: -(α)4.9 from a Current Multiplex Gap-Polymerase Chain Reaction

The Characteristics of Compound Heterozygosity for Hemoglobin G-Makassar with Hb E in Malaysia

A rare case of compound heterozygous Southeast Asian double α-globin gene deletion and Haemoglobin Quong Sze in a Malay proband

Suchergebnisse filtern