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Journal Articles

Characterisation of Three Unique Head-to-Tail Alpha Globin Cluster Duplications Contributing to Beta Thalassemia Intermedia in 3 Families

Blood (2015) 126 (23): 3375.

https://doi.org/10.1182/blood.V126.23.3375.3375

Published: 2015

Journal Articles

The LRF/ZBTB7A Transcription Factor Is a BCL11A-Independent Repressor of Fetal Hemoglobin

Blood (2015) 126 (23): 2.

https://doi.org/10.1182/blood.V126.23.2.2

Published: 2015

Journal Articles

Wide Spectrum of Molecular and Clinical Heterogeneity in HbH Disease in North Indian Patients

Reena Das, MD, Chris Fisher, PhD, Jasbir Kaur, BSc, Ayyub Helena, BSc, Amita Trehan, MD, Deepak Bansal, MD, Prashant Sharma, MD DNB, DM, Pankaj Malhotra, MBBS, MD, Higgs Douglas, MD, David J Weatherall, FRS

Blood (2014) 124 (21): 1358.

https://doi.org/10.1182/blood.V124.21.1358.1358

Published: 2014

Journal Articles

Mutations in Krüppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression

Vip Viprakasit, Supachai Ekwattanakit, Suchada Riolueang, Nipon Chalaow, Chris Fisher, Karen Lower, Hitoshi Kanno, Kalaya Tachavanich, Sasithorn Bejrachandra, Jariya Saipin, Monthana Juntharaniyom, Kleebsabai Sanpakit, Voravarn S. Tanphaichitr, Duantida Songdej, Christian Babbs, Richard J. Gibbons, Sjaak Philipsen, Douglas R. Higgs

Blood (2014) 123 (10): 1586–1595.

https://doi.org/10.1182/blood-2013-09-526087

Published: 2014

Includes: Supplemental data

Journal Articles

Analysis of JAK3 , JAK2 , and C-MPL mutations in transient myeloproliferative disorder and myeloid leukemia of Down syndrome blasts in children with Down syndrome

Alice Norton, Chris Fisher, Hui Liu, Qiang Wen, Gina Mundschau, Jose Luis Fuster, Henrik Hasle, Bernward Zeller, David K. Webb, Aengus O'Marcaigh, April Sorrell, Joanne Hilden, Alan Gamis, John D. Crispino, Paresh Vyas

Blood (2007) 110 (3): 1077–1079.

https://doi.org/10.1182/blood-2007-03-080374

Published: 2007

Journal Articles

Two Novel Somatic Mutations of the ATRX Gene in Female Patients with Acquired Alpha Thalassemia of Myelodysplastic Syndrome (ATMDS).

Peter S. Haas, MD, Michael Schwabe, MD, Chris Fisher, MD, PhD, Richard Gibbons, MD, Doug R. Higgs, MD, Emanuel Bissé, MD, Michael Lübbert, MD, PhD

Blood (2006) 108 (11): 1765.

https://doi.org/10.1182/blood.V108.11.1765.1765

Published: 2006

Journal Articles

Analysis of GATA-1 Mutations in Chronic Myeloid Leukaemia.

Christina Halsey, Chris Fisher, Brenda Gibson, Paresh Vyas, Gerry Graham

Blood (2006) 108 (11): 4774.

https://doi.org/10.1182/blood.V108.11.4774.4774

Published: 2006

NARROW

Characterisation of Three Unique Head-to-Tail Alpha Globin Cluster Duplications Contributing to Beta Thalassemia Intermedia in 3 Families

The LRF/ZBTB7A Transcription Factor Is a BCL11A-Independent Repressor of Fetal Hemoglobin

Wide Spectrum of Molecular and Clinical Heterogeneity in HbH Disease in North Indian Patients

Mutations in Krüppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression

Analysis of JAK3 , JAK2 , and C-MPL mutations in transient myeloproliferative disorder and myeloid leukemia of Down syndrome blasts in children with Down syndrome

Two Novel Somatic Mutations of the ATRX Gene in Female Patients with Acquired Alpha Thalassemia of Myelodysplastic Syndrome (ATMDS).

Analysis of GATA-1 Mutations in Chronic Myeloid Leukaemia.

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ASH Publications

American Society of Hematology

Characterisation of Three Unique Head-to-Tail Alpha Globin Cluster Duplications Contributing to Beta Thalassemia Intermedia in 3 Families

The LRF/ZBTB7A Transcription Factor Is a BCL11A-Independent Repressor of Fetal Hemoglobin

Wide Spectrum of Molecular and Clinical Heterogeneity in HbH Disease in North Indian Patients

Mutations in Krüppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression

Analysis of JAK3 , JAK2 , and C-MPL mutations in transient myeloproliferative disorder and myeloid leukemia of Down syndrome blasts in children with Down syndrome

Two Novel Somatic Mutations of the ATRX Gene in Female Patients with Acquired Alpha Thalassemia of Myelodysplastic Syndrome (ATMDS).

Analysis of GATA-1 Mutations in Chronic Myeloid Leukaemia.

Email alerts

ASH Publications

American Society of Hematology

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