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    Andrea Quintana, Matthew J. Garabedian, Robert J. Wallerstein, Antenatal detection of maternal unipartental disomy of chromosome 2 in a fetus with non-chromosomal, non-syndromic alobar holoprosencephaly, American Journal of Medical Genetics Part A, 2014, 164, 1
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    Q. Ding, Y. Shen, L. Yang, X. Wang, A. R. Rezaie, The missense Thr211Pro mutation in the factor X activation peptide of a bleeding patient causes molecular defect in the clotting cascade, Thrombosis and Haemostasis, 2013, 110, 1, 53

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