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Hemoglobin|May 1, 1995
A novel frameshift mutation causing beta-thalassemia in a SikhS el-Kalla, A R MathewsHemoglobin|August 1, 1993
Molecular characterization of beta-thalassemia in the United Arab EmiratesS el-Kalla, A R MathewsHemoglobin|May 1, 1997
A significant beta-thalassemia heterogeneity in the United Arab EmiratesS el-Kalla, A R MathewsAsia-Oceania Journal of Obstetrics and Gynaecology|March 1, 1990
Current method for first and second trimester prenatal diagnosis: transabdominal chorionic villi samplingK Buckshee, S Parveen, I C VermaIndian Journal of Pediatrics|March 29, 2003
Genetic counseling in acrocallosal syndromeSunita Bijarnia, Ashok Baijal, I C VermaIndian Pediatrics|September 1, 1992
Congenital heart disease in Down syndrome: an echocardiographic studyS Bhatia, I C Verma, S ShrivastavaBulletin of the World Health Organization|January 1, 1991
How long after being collected can blood still be cultured for chromosomal studies in the tropicsR Elango, S Mathew, I C VermaThe Indian Journal of Medical Research|June 1, 1997
Detection of beta-thalassaemia mutation insertion ATCT at codon 47/48 by ARMS technique for screening & prenatal diagnosisR Saxena, E Thomas, I C VermaIndian Journal of Pediatrics|May 8, 2000
Development and assessment of a screening test for detecting childhood disabilitiesG Chopra, I C Verma, P SeetharamanAmerican Journal of Medical Genetics|July 1, 1994
Blepharophimosis, telecanthus, microstomia, and unusual ear anomaly (Simosa syndrome) in an infantM Suri, M Kabra, I C VermaPageof 14