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Q37172916-29A1D158-9457-49A8-AAF9-76D6E0ED181A
Q37172916-29A1D158-9457-49A8-AAF9-76D6E0ED181A
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http://www.wikidata.org/entity/statement/Q37172916-29A1D158-9457-49A8-AAF9-76D6E0ED181A
The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.
P2860
Q37172916-29A1D158-9457-49A8-AAF9-76D6E0ED181A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37172916-29A1D158-9457-49A8-AAF9-76D6E0ED181A
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wasDerivedFrom
67d40bb1db91a8a1a14963aad1a8b2ff30deb5c8
P2860
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype