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Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation.

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Title: Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation.
Authors: Netravathi, Manjunath1, Kumari, Renu2, Kapoor, Saketh3, Dakle, Pushkar2, Dwivedi, Manish Kumar2, Roy, Sumitabho Deb4, Pandey, Paritosh5, Saini, Jitender6, Ramakrishna, Anil1, Navalli, Devaraddi1, Satishchandra, Parthasarathy1, Pal, Pramod Kumar1 pal.pramod@rediffmail.com, Kumar, Arun3 karun@mrdg.jisc.ernet.in, Faruq, Mohammed2 faruq.mohd@igib.res.in
Source: BMC Medical Genetics. 2015, Vol. 16 Issue 1, p1-8. 8p.
Database: Academic Search Ultimate
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  Data: Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation.
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  Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genetics%22">BMC Medical Genetics</searchLink>. 2015, Vol. 16 Issue 1, p1-8. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=101976591
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        Value: 10.1186/s12881-015-0151-8
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        Text: English
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        PageCount: 8
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      – TitleFull: Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation.
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              Text: 2015
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