Resultados de búsqueda - Sunita Bijarnia-Mahay

Weill-Marchesani syndrome: A rare cause of ectopia lentis and short stature por Sapna Sandal, Varshini Shanker, Swasti Pal, Sunita Bijarnia-Mahay

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Prenatal presentation of a rare genetic disorder: a clinical, autopsy and molecular correlation por Veronica Arora, Sunita Bijarnia-Mahay, Samarth Kulshreshtra, Kanika Singh, Ratna Dua Puri, Ishwar Chandar Verma

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Mutation-proved Clouston syndrome in a large Indian family with a variant phenotype por Sangeeta Khatter, Ratna Dua Puri, Sunita Bijarnia Mahay, Pratibha Bhai, Renu Saxena, Ishwar C Verma

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NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results - a pilot study por Kanika Singh, Sunita Bijarnia-Mahay, V. L. Ramprasad, Ratna Dua Puri, Sandhya Nair, Sheetal Sharda, Renu Saxena, Sudha Kohli, Samarth Kulshreshtha, Indrani Ganguli, Kanwal Gujral, Ishwar C. Verma

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