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Journal Articles

The Occurrence of Mutations in PTPN11 and KRAS Is Not Dissimilar in Patients with Indolent Juvenile Myelomonocytic Leukemia (JMML) from Those with Clinically More Aggressive Disease.

Anupama G. Rao, MRCPCH, MRCPath, Phil J. Ancliff, MRCP MRCPath, David K. Webb, FRCP FRCPath, David C. Linch, FRCPath, Rosemary E. Gale, PhD

Blood (2007) 110 (11): 2424.

https://doi.org/10.1182/blood.V110.11.2424.2424

Published: 2007

Journal Articles

Identification of Two Novel Homozygous HAX1 Mutations in an Autosomal Recessive Jewish and Two Unrelated Sporadic British Families with Severe Congenital Neutropenia.

Bradley N. Smith, PhD, Phil J. Ancliff, MRCPath, David C. Linch, FRCPath, Rosemary E. Gale, PhD

Blood (2007) 110 (11): 3309.

https://doi.org/10.1182/blood.V110.11.3309.3309

Published: 2007

Journal Articles

Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia

Phil J. Ancliff, Michael P. Blundell, Giles O. Cory, Yolanda Calle, Austen Worth, Helena Kempski, Siobhan Burns, Gareth E. Jones, Jo Sinclair, Christine Kinnon, Ian M. Hann, Rosemary E. Gale, David C. Linch, Adrian J. Thrasher

Blood (2006) 108 (7): 2182–2189.

https://doi.org/10.1182/blood-2006-01-010249

Published: 2006

Includes: Multimedia, Supplemental data

Journal Articles

Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia

Phil J. Ancliff, Rosemary E. Gale, Michael J. Watts, Ri Liesner, Ian M. Hann, Stephan Strobel, David C. Linch

Blood (2002) 100 (2): 707–709.

https://doi.org/10.1182/blood-2002-01-0060

Published: 2002

Journal Articles

Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease

Phil J. Ancliff, Rosemary E. Gale, Ri Liesner, Ian M. Hann, David C. Linch

Blood (2001) 98 (9): 2645–2650.

https://doi.org/10.1182/blood.V98.9.2645

Published: 2001

NARROW

The Occurrence of Mutations in PTPN11 and KRAS Is Not Dissimilar in Patients with Indolent Juvenile Myelomonocytic Leukemia (JMML) from Those with Clinically More Aggressive Disease.

Identification of Two Novel Homozygous HAX1 Mutations in an Autosomal Recessive Jewish and Two Unrelated Sporadic British Families with Severe Congenital Neutropenia.

Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia

Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia

Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease

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ASH Publications

American Society of Hematology

The Occurrence of Mutations in PTPN11 and KRAS Is Not Dissimilar in Patients with Indolent Juvenile Myelomonocytic Leukemia (JMML) from Those with Clinically More Aggressive Disease.

Identification of Two Novel Homozygous HAX1 Mutations in an Autosomal Recessive Jewish and Two Unrelated Sporadic British Families with Severe Congenital Neutropenia.

Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia

Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia

Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease

Email alerts

ASH Publications

American Society of Hematology

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