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Q40997916-0EF583CF-83EF-4F91-9E64-C07734F8DA5F
Q40997916-0EF583CF-83EF-4F91-9E64-C07734F8DA5F
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http://www.wikidata.org/entity/statement/Q40997916-0EF583CF-83EF-4F91-9E64-C07734F8DA5F
Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
P2860
Q40997916-0EF583CF-83EF-4F91-9E64-C07734F8DA5F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40997916-0EF583CF-83EF-4F91-9E64-C07734F8DA5F
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wasDerivedFrom
6d66e57e521882642dd0d1f25c0305f1248863a5
P2860
Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports.