FAN XIA to Chromosomes, Human, Pair 15
This is a "connection" page, showing publications FAN XIA has written about Chromosomes, Human, Pair 15.
Connection Strength
0.055
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The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families. Genet Med. 2017 01; 19(1):45-52.
Score: 0.030
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Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. Nat Genet. 2013 Nov; 45(11):1405-8.
Score: 0.025