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Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis and polydactyly

Anjana Kar, Shubha R Phadke, Aneek Das Bhowmik, Ashwin Dalal
doi: https://doi.org/10.1101/109124
Anjana Kar
1Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India;
2Graduate Studies, Manipal University, Manipal, India;
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Shubha R Phadke
3Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India;
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Aneek Das Bhowmik
2Graduate Studies, Manipal University, Manipal, India;
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Ashwin Dalal
1Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India;
4Department of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, India.
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  • For correspondence: ashwindalal@gmail.com adalal@cdfd.org.in
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Posted February 17, 2017.
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Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis and polydactyly
Anjana Kar, Shubha R Phadke, Aneek Das Bhowmik, Ashwin Dalal
bioRxiv 109124; doi: https://doi.org/10.1101/109124
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Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis and polydactyly
Anjana Kar, Shubha R Phadke, Aneek Das Bhowmik, Ashwin Dalal
bioRxiv 109124; doi: https://doi.org/10.1101/109124

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