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Journal Articles

The Occurrence of Four Globin Abnormalities in One Individual: Hb SC Disease with Hb Chicago and Deletional Alpha Thalassemia.

Heather Hughes, Ferdane Kutlar, MD, Kathleen M. McKie, MD, Leslie Holley, Dedrey Elam, Abdullah Kutlar, MD

Blood (2007) 110 (11): 3802.

https://doi.org/10.1182/blood.V110.11.3802.3802

Published: 2007

Journal Articles

Mu Opioid Receptor (OPRM-1) Polymorphisms among Patients with Sickle Cell Disease.

Sharmila Mehta, MD, Nicholas Campbell, Lakiea Bailey, Ferdane Kutlar, MD, Dedrey Elam, Betsy Clair, Abdullah Kutlar, MD

Blood (2005) 106 (11): 3804.

https://doi.org/10.1182/blood.V106.11.3804.3804

Published: 2005

Journal Articles

Haptoglobin Genotypes among Pediatric and Adult Sickle Cell Patients: An Emerging Genetic Modifier?.

Heather Y. Hughes, Ferdane Kutlar, MD, Betsy Clair, Dedrey Elam, Kathleen M. McKie, MD, Abdullah Kutlar, MD

Blood (2005) 106 (11): 3805.

https://doi.org/10.1182/blood.V106.11.3805.3805

Published: 2005

Journal Articles

Neonatal Cyanosis Due to a Novel Fetal M-Hemoglobin: Hemoglobin F-M Circleville (Gγ63 His→Leu).

Ferdane Kutlar, MD, Richard Shell, MD, Joan Atkin, MD, Dedrey Elam, Leslie Holley, Deborah Davis, Jeanette Harbin, Abdullah Kutlar, MD

Blood (2005) 106 (11): 3806.

https://doi.org/10.1182/blood.V106.11.3806.3806

Published: 2005

Journal Articles

Atypical Hemoglobin H Disease Due to Compound Heterozygosity for -α 3.7 and --SEA Deletions and Heterozygosity for the β-Chain Variant Hemoglobin Raleigh (β1 VAL→ALA).

Ferdane Kutlar, MD, Mary Ann Knovich, MD, Dedrey Elam, Daniel B. Jobe, MD, David H. Buss, MD, Jeanette Harbin, Deborah H. Davis, Hernon Sabio, MD, Abdullah Kutlar, MD

Blood (2005) 106 (11): 3849.

https://doi.org/10.1182/blood.V106.11.3849.3849

Published: 2005

Journal Articles

The Influence of Uridine Diphosphate Glucuronosyl Transferase 1A Promoter Polymorphism, β S -Globin Gene Haplotype, Co-Inherited α-Thalassemia Trait and Hb F on Steady-State Serum Bilirubin Levels in Sickle Cell Anemia.

Adekunle D. Adekile, MD, PhD, Ferdane Kutlar, MD, Kathleen McKie, MD, Anthony Addington, Dedrey Elam, Betsy Clair, Leslie Holley, Abdullah Kutlar, MD.

Blood (2004) 104 (11): 1682.

https://doi.org/10.1182/blood.V104.11.1682.1682

Published: 2004

NARROW

The Occurrence of Four Globin Abnormalities in One Individual: Hb SC Disease with Hb Chicago and Deletional Alpha Thalassemia.

Mu Opioid Receptor (OPRM-1) Polymorphisms among Patients with Sickle Cell Disease.

Haptoglobin Genotypes among Pediatric and Adult Sickle Cell Patients: An Emerging Genetic Modifier?.

Neonatal Cyanosis Due to a Novel Fetal M-Hemoglobin: Hemoglobin F-M Circleville (Gγ63 His→Leu).

Atypical Hemoglobin H Disease Due to Compound Heterozygosity for -α 3.7 and --SEA Deletions and Heterozygosity for the β-Chain Variant Hemoglobin Raleigh (β1 VAL→ALA).

The Influence of Uridine Diphosphate Glucuronosyl Transferase 1A Promoter Polymorphism, β S -Globin Gene Haplotype, Co-Inherited α-Thalassemia Trait and Hb F on Steady-State Serum Bilirubin Levels in Sickle Cell Anemia.

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ASH Publications

American Society of Hematology

The Occurrence of Four Globin Abnormalities in One Individual: Hb SC Disease with Hb Chicago and Deletional Alpha Thalassemia.

Mu Opioid Receptor (OPRM-1) Polymorphisms among Patients with Sickle Cell Disease.

Haptoglobin Genotypes among Pediatric and Adult Sickle Cell Patients: An Emerging Genetic Modifier?.

Neonatal Cyanosis Due to a Novel Fetal M-Hemoglobin: Hemoglobin F-M Circleville (Gγ63 His→Leu).

Atypical Hemoglobin H Disease Due to Compound Heterozygosity for -α 3.7 and --SEA Deletions and Heterozygosity for the β-Chain Variant Hemoglobin Raleigh (β1 VAL→ALA).

The Influence of Uridine Diphosphate Glucuronosyl Transferase 1A Promoter Polymorphism, β S -Globin Gene Haplotype, Co-Inherited α-Thalassemia Trait and Hb F on Steady-State Serum Bilirubin Levels in Sickle Cell Anemia.

Email alerts

ASH Publications

American Society of Hematology

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