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Y. Tsurusaki, R. Yonezawa, M. Furuya, G. Nishimura, R.K. Pooh, M. Nakashima, H. Saitsu, N. Miyake, S. Saito and N. Matsumoto Whole exome sequencing revealed biallelic IFT122 mutations in a family with CED1 and recurrent pregnancy loss Clinical Genetics 85

Article first published online: 5 JUL 2013 | DOI: 10.1111/cge.12215

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