Connection
Emily Farrow to Microcephaly
This is a "connection" page, showing publications Emily Farrow has written about Microcephaly.
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0.120 |
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Dinwiddie DL, Soden SE, Saunders CJ, Miller NA, Farrow EG, Smith LD, Kingsmore SF. De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies. BMC Med Genomics. 2013 Sep 17; 6:32.
Score: 0.120