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American Journal of Medical Genetics|October 1, 1994
Poland anomaly with unusual associated anomalies: case report of an apparent disorganized defectM Kabra, M Suri, U Jain, et al.
Indian Journal of Nephrology|January 17, 2019
Autosomal Dominant Polycystic Kidney Disease: Presence of Hypomorphic Alleles in PKD1 GeneS Pandita, D Khullar, R Saxena, et al.
Indian Pediatrics|May 1, 1990
Prenatal diagnosis of chromosomal disorders in DelhiI C Verma, S Mathew, R Elango, et al.
Indian Pediatrics|September 1, 1991
Cytogenetic studies in Down syndromeI C Verma, S Mathew, R Elango, et al.
Clinical Genetics|January 1, 1976
Split-hand and split-foot deformity inherited as an autosomal recessive traitI C Verma, R Joseph, S Bhargava, et al.
Cardiology Research and Practice|November 24, 2011
Premature coronary artery disease and familial hypercholesterolemia: need for early diagnosis and cascade screening in the Indian populationN Setia, I C Verma, B Khan, et al.
The Indian Journal of Medical Research|March 1, 1996
Cytogenetic studies in ataxia telangiectasia & their use in prenatal diagnosisM R Chowdhury, G Singh, A Shukla, et al.
Prenatal Diagnosis|March 4, 1998
Prenatal diagnosis of beta-thalassaemia: experience in a developing countryR Saxena, P K Jain, E Thomas, et al.
Indian Journal of Pediatrics|March 1, 1996
Cystic fibrosis--an Indian perspective on recent advances in diagnosis and managementS K Kabra, M Kabra, M Ghosh, et al.
Indian Pediatrics|October 14, 2011
Congenital hyperinsulinism caused by mutations in ABCC8 (SUR1) geneSeema Thakur, Sarah E Flanagan, Sian Ellard, et al.
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