Published in

Wiley, The American Journal of Medical Genetics - Part A, 1(176), p. 34-40, 2017

DOI: 10.1002/ajmg.a.38537

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

Journal article published in 2017 by Anjana Kar, Shubha R. Phadke ORCID, Aneek Das Bhowmik, Aneek Das Bhowmik ORCID, Ashwin Dalal ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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