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Netravathi, Manjunath and Kumari, Renu and Kapoor, Saketh and Dakle, Pushkar and Dwivedi, Manish Kumar and Roy, Sumitabho Deb and Pandey, Paritosh and Saini, Jitender and Ramakrishna, Anil and Navalli, Devaraddi and Satishchandra, Parthasarathy and Pal, Pramod Kumar and Kumar, Arun and Faruq, Mohammed (2015) Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. In: BMC MEDICAL GENETICS, 16 .