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1
Q42740182-DAC43E86-0EB0-4882-8774-CB393FEB63DB
Q42740182-DAC43E86-0EB0-4882-8774-CB393FEB63DB
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Statement
http://www.wikidata.org/entity/statement/Q42740182-DAC43E86-0EB0-4882-8774-CB393FEB63DB
Clinical features and an atypical WT1 mutant site in a child with incomplete Denys-Drash syndrome.
P2860
Q42740182-DAC43E86-0EB0-4882-8774-CB393FEB63DB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42740182-DAC43E86-0EB0-4882-8774-CB393FEB63DB
rank
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type
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wasDerivedFrom
ca2160acbd866a765470d11c50312699b7186b83
P2860
An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.