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Q43818868-4D4FFA8D-34A2-494D-B24E-13D26ED09B92
Q43818868-4D4FFA8D-34A2-494D-B24E-13D26ED09B92
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43818868-4D4FFA8D-34A2-494D-B24E-13D26ED09B92
Ovarian failure in HAX1-deficient patients: is there a gender-specific difference in pubertal development in severe congenital neutropenia or Kostmann disease?
P2860
Q43818868-4D4FFA8D-34A2-494D-B24E-13D26ED09B92
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43818868-4D4FFA8D-34A2-494D-B24E-13D26ED09B92
rank
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type
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wasDerivedFrom
4c16c1db28a015ab0a3f3e1ccafaf3e1e33cc4d6
P2860
Infantile genetic agranulocytosis, morbus Kostmann: presentation of six cases from the original "Kostmann family" and a review.