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Q37223716-7F871340-4F6D-4BC7-A9B8-E7BFD4DD4F0B
Q37223716-7F871340-4F6D-4BC7-A9B8-E7BFD4DD4F0B
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Statement
http://www.wikidata.org/entity/statement/Q37223716-7F871340-4F6D-4BC7-A9B8-E7BFD4DD4F0B
Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene.
P2860
Q37223716-7F871340-4F6D-4BC7-A9B8-E7BFD4DD4F0B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37223716-7F871340-4F6D-4BC7-A9B8-E7BFD4DD4F0B
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wasDerivedFrom
fafb5f772a742b468fca3bd6b134de590c207a22
P2860
Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease.