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Journal Articles

Possible Perforin-Munc13-4 Gene-Gene Interaction in Familial Hemophagocytic Lymphohistiocytosis

Gunay Balta, Hamza Okur, Nurten Akarsu, Sule Unal, Cigdem Altay, Aytemiz Gurgey

Blood (2008) 112 (11): 4643.

https://doi.org/10.1182/blood.V112.11.4643.4643

Published: 2008

Journal Articles

Molecular Characterization of a Prototype Family Harboring Two Genomic Instability Disorders: Ataxia Telangiectasia and Fanconi Anemia.

Gunay Balta, Turkan Patiroglu, Fatma Gumruk, Ozden Sanal, Aytemiz Gurgey, Cigdem Altay

Blood (2007) 110 (11): 1680.

https://doi.org/10.1182/blood.V110.11.1680.1680

Published: 2007

Journal Articles

A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis

E. Jennifer Edelman, Yelena Maksimova, Feride Duru, Cigdem Altay, Patrick G. Gallagher

Blood (2007) 109 (12): 5491–5493.

https://doi.org/10.1182/blood-2006-09-046573

Published: 2007

Includes: Supplemental data

Journal Articles

Pyrimidine 5′ Nucleotidase-1 (P5N-1) Deficiency Associated with 4 Novel Mutations in 5 New Turkish Families: Genotype-Phenotype Analysis.

Gunay Balta, PhD, Aytemiz Gurgey, MD, Fatma Gumruk, MD, Yahya Buyukasik, MD, Meral Beksac, MD, Cigdem Altay, MD

Blood (2006) 108 (11): 3743.

https://doi.org/10.1182/blood.V108.11.3743.3743

Published: 2006

Journal Articles

Molecular characterization of Turkish patients with pyrimidine 5′ nucleotidase-I deficiency

Gunay Balta, Fatma Gumruk, Nurten Akarsu, Aytemiz Gurgey, Cigdem Altay

Blood (2003) 102 (5): 1900–1903.

https://doi.org/10.1182/blood-2003-02-0628

Published: 2003

Journal Articles

Association of complementation group and mutation type with clinical outcome in Fanconi anemia

Blood (2000) 96 (13): 4064–4070.

https://doi.org/10.1182/blood.V96.13.4064

Published: 2000

Journal Articles

Normal and Variant Isoenzymes of Human Blood Cell Hexokinase and the Isoenzyme Patterns in Hemolytic Anemia

CIGDEM ALTAY, CHESTER A. ALPER, DAVID G. NATHAN

Blood (1970) 36 (2): 219–227.

https://doi.org/10.1182/blood.V36.2.219.219

Published: 1970

NARROW

Possible Perforin-Munc13-4 Gene-Gene Interaction in Familial Hemophagocytic Lymphohistiocytosis

Molecular Characterization of a Prototype Family Harboring Two Genomic Instability Disorders: Ataxia Telangiectasia and Fanconi Anemia.

A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis

Pyrimidine 5′ Nucleotidase-1 (P5N-1) Deficiency Associated with 4 Novel Mutations in 5 New Turkish Families: Genotype-Phenotype Analysis.

Molecular characterization of Turkish patients with pyrimidine 5′ nucleotidase-I deficiency

Association of complementation group and mutation type with clinical outcome in Fanconi anemia

Normal and Variant Isoenzymes of Human Blood Cell Hexokinase and the Isoenzyme Patterns in Hemolytic Anemia

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ASH Publications

American Society of Hematology

Possible Perforin-Munc13-4 Gene-Gene Interaction in Familial Hemophagocytic Lymphohistiocytosis

Molecular Characterization of a Prototype Family Harboring Two Genomic Instability Disorders: Ataxia Telangiectasia and Fanconi Anemia.

A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis

Pyrimidine 5′ Nucleotidase-1 (P5N-1) Deficiency Associated with 4 Novel Mutations in 5 New Turkish Families: Genotype-Phenotype Analysis.

Molecular characterization of Turkish patients with pyrimidine 5′ nucleotidase-I deficiency

Association of complementation group and mutation type with clinical outcome in Fanconi anemia

Normal and Variant Isoenzymes of Human Blood Cell Hexokinase and the Isoenzyme Patterns in Hemolytic Anemia

Email alerts

ASH Publications

American Society of Hematology

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