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Q52681131-0CD4C513-185B-4153-9197-A9A69130739E
Q52681131-0CD4C513-185B-4153-9197-A9A69130739E
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http://www.wikidata.org/entity/statement/Q52681131-0CD4C513-185B-4153-9197-A9A69130739E
Demonstration of a novel Xp22.2 microdeletion as the cause of familial extreme skewing of X-inactivation utilizing case-parent trio SNP microarray analysis.
P2860
Q52681131-0CD4C513-185B-4153-9197-A9A69130739E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52681131-0CD4C513-185B-4153-9197-A9A69130739E
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wasDerivedFrom
60a1946a98f25d7f603e1e4d34ecd4605f9f5223
P2860
Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita