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American Journal of Medical Genetics|March 1, 1992
del(18p) syndrome with complex tetralogy of Fallot in an infant with 45,X,t(Y;18)(q12;q11.2)S el Kalla, A R Mathews, N S Menon
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.
Ophthalmic Paediatrics and Genetics|December 1, 1991
Microphthalmos and anterior segment dysgenesis in a familyS Ghose, N P Singh, D Kaur, et al.
Human Genetics|July 1, 1997
Regional distribution of beta-thalassemia mutations in IndiaI C Verma, R Saxena, E Thomas, et al.
Indian Pediatrics|August 18, 2014
Mitochondrial DNA depletion syndrome causing liver failureSunita Bijarnia-Mahay, Neelam Mohan, Deepak Goyal, et al.
Indian Journal of Pediatrics|September 1, 1996
Management of Wiskott-Aldrich syndromeA Srivastava, H A Swaid, M Kabra, et al.
Indian Journal of Pediatrics|March 1, 1991
Facial anthropometry in newborns in PondicherryM Shah, I C Verma, S Mahadevan, et al.
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