R. Kumar

发表

Association and interaction of the TNF-alpha gene with other pro- and anti-inflammatory cytokine genes and HLA genes in patients with type 1 diabetes from North India.

S. K. Singh, R. Goswami, N. Israni, 2007, Tissue antigens.

A Case of Guillain Barre Syndrome Complicated By pANCA Positivity , Elevated CSF Sugar and Protein with Decreased 25 Hydroxy ( OH ) Vitamin D And B 12 Levels

Vanitha Muralikumar, R. Kumar, I. Jyothi, 2016 .

Molecular characterization of native chicken: prospects and challenges

S. Prasad, R. Kumar, S. Agarwal, 2020 .

Clinical and haematological features in a compound heterozygote (HBB:c.92 + 5G > C/HBB:c.93‐2A > C) case of thalassaemia major

S. Agarwal, P. Tamhankar, R. Kumar, 2010, International journal of laboratory hematology.

Association of 5, 10- methylenetetrahydrofolate reductase C677T polymorphism in susceptibility to tropical chronic pancreatitis in north Indian population.

G. Choudhuri, R. Kumar, S. Agarwal, 2012, Cellular and molecular biology.

Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21.

C. Woods, J. Tolmie, H. Brunner, 2000, American journal of human genetics.

Nonsense mutation of β‐globin gene at codon 82 (AAG→TAG) or HBB:C247 A→T with polymorphism: cause of thalassemia intermedia?

S. Agarwal, R. Kumar, 2011, International journal of laboratory hematology.

A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma

S. Bhattacharya, A. Moore, P. Francis, 2003, The British journal of ophthalmology.

Post-transfusion purpura: case report

A. Ghali, R. Kumar, A. Ekaldious, 2001, Annals of Hematology.

Pregnancy induced hemolytic anemia: an unexplained entity

A. Advani, J. Sharan, R. Kumar, 2001, Annals of Hematology.