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Journal Articles

Fluorescent PCR Based Gene Dose Assessment for Detection of Deletion Mutations in the FIX Gene Among Carriers of Hemophilia B.

Eunice Sindhuvi Edison, Ph.D, G. Sankari Devi, B.Sc, G. Jayandharan, Ph.D, Shaji R Velayudhan, Ph.D, Auro Viswabandya, MD, Vikram Mathews, MD, Mammen Chandy, MD, Alok Srivastava, MD

Blood (2009) 114 (22): 3486.

https://doi.org/10.1182/blood.V114.22.3486.3486

Published: 2009

Journal Articles

Polymorphisms in Coagulant and Inflammatory Genes Modify the Phenotype of Severe Hemophilia A and B.

G. Jayandharan, Mercy Devadharshini, Auro Viswabandya, Sukesh C. Nair, R.V. Shaji, Vikram Mathews, Mammen Chandy, Alok Srivastava

Blood (2006) 108 (11): 1009.

https://doi.org/10.1182/blood.V108.11.1009.1009

Published: 2006

Journal Articles

Two Mutations (1717 T〉C, GP IX;124del145, GPIb beta) Occur Frequently among Patients with Bernard Soulier Syndrome in India.

Rintu Rebecca Jacob, G. Jayandharan, Auro Viswabandya, Shoma Baidya, Sukesh C. Nair, Biju George, Vikram Mathews, Mammen Chandy, Alok Srivastava

Blood (2006) 108 (11): 1096.

https://doi.org/10.1182/blood.V108.11.1096.1096

Published: 2006

Journal Articles

Six Novel Mutations Including Triple Heterozygosity for Phe31Ser, 514delT and 516T→G Mutations in Factor X Gene Is Responsible for Congenital Factor X Deficiency in Patients of Indian and Nepali Origin.

G Jayandharan, RV Shaji, Auro Viswabandhya, Sukesh C. Nair, Joy Mammen, Biju George, Vikram Mathews, Mammen Chandy, Alok Srivastava

Blood (2004) 104 (11): 1042.

https://doi.org/10.1182/blood.V104.11.1042.1042

Published: 2004

Journal Articles

Molecular Genetics of Hereditary Prothrombin Deficiency in Indian Patients: Identification of a Novel Ala362→Thr (Prothrombin Vellore 1) Mutation by Conformation Sensitive Gel Electrophoresis.

G Jayandharan, R.V. Shaji, Auro Viswabandhya, Sukesh C. Nair, Joy Mammen, Biju George, Vikram Mathews, Mammen Chandy, Alok Srivastava

Blood (2004) 104 (11): 1037.

https://doi.org/10.1182/blood.V104.11.1037.1037

Published: 2004

NARROW

Fluorescent PCR Based Gene Dose Assessment for Detection of Deletion Mutations in the FIX Gene Among Carriers of Hemophilia B.

Polymorphisms in Coagulant and Inflammatory Genes Modify the Phenotype of Severe Hemophilia A and B.

Two Mutations (1717 T〉C, GP IX;124del145, GPIb beta) Occur Frequently among Patients with Bernard Soulier Syndrome in India.

Six Novel Mutations Including Triple Heterozygosity for Phe31Ser, 514delT and 516T→G Mutations in Factor X Gene Is Responsible for Congenital Factor X Deficiency in Patients of Indian and Nepali Origin.

Molecular Genetics of Hereditary Prothrombin Deficiency in Indian Patients: Identification of a Novel Ala362→Thr (Prothrombin Vellore 1) Mutation by Conformation Sensitive Gel Electrophoresis.

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ASH Publications

American Society of Hematology

Fluorescent PCR Based Gene Dose Assessment for Detection of Deletion Mutations in the FIX Gene Among Carriers of Hemophilia B.

Polymorphisms in Coagulant and Inflammatory Genes Modify the Phenotype of Severe Hemophilia A and B.

Two Mutations (1717 T〉C, GP IX;124del145, GPIb beta) Occur Frequently among Patients with Bernard Soulier Syndrome in India.

Six Novel Mutations Including Triple Heterozygosity for Phe31Ser, 514delT and 516T→G Mutations in Factor X Gene Is Responsible for Congenital Factor X Deficiency in Patients of Indian and Nepali Origin.

Molecular Genetics of Hereditary Prothrombin Deficiency in Indian Patients: Identification of a Novel Ala362→Thr (Prothrombin Vellore 1) Mutation by Conformation Sensitive Gel Electrophoresis.

Email alerts

ASH Publications

American Society of Hematology

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