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Mutation Research|April 1, 1989
Different mutations responsible for the elevated sister-chromatid exchange frequencies in Bloom syndrome and X-irradiated B-lymphoblastoid cell lines originating from acute leukemiaY Shiraishi, T Taguchi, M Ozawa, et al.
Human Genetics|July 1, 1997
Association of polymorphism at COL3A and CTLA4 loci on chromosome 2q31-33 with the clinical phenotype and in-vitro CMI status in healthy and leprosy subjects: a preliminary studyG Kaur, G Sachdeva, L K Bhutani, et al.
Clinical Genetics|August 1, 1984
Genetics of site specific colon cancer: a family studyR Bamezai, G Singh, N N Khanna, et al.
Human Genetics|July 1, 1997
Genetic variations at the T cell receptor gamma locus in circulating peripheral blood mononuclear cells of clinically categorised leprosy patientsG Sachdeva, G Kaur, L K Bhutani, et al.
DNA and Cell Biology|August 6, 2004
Dominant negative effect of novel mutations in pyruvate kinase-M2M Anitha, G Kaur, N Z Baquer, et al.
Annales De Genetique|June 9, 2004
A novel promoter polymorphism (-71C>T) in KRTHB6 gene in Indian populationNarendra K Bairwa, Dheeraj Malhotra, Anjana Saha, et al.
Human Genetics|August 30, 1976
A familial tetraphocomelia syndrome involving limb deformities, cleft lip, cleft palate, and associated anomalies--a new syndromeK Kucheria, S K Bhargava, R Bamezai, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|December 17, 2003
Two novel somatic mutations in the human interleukin 6 promoter region in a patient with sporadic breast cancerA Saha, N K Bairwa, A Ranjan, et al.
Clinical Genetics|March 1, 1987
Cerebellar ataxia and total albinismR Bamezai, S A Husain, S Misra, et al.
Annales De Genetique|March 31, 2004
A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian originSujay Khandpur, N K Bairwa, B S N Reddy, et al.
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