PMC:1440874 / 996-1222 JSONTXT

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{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T136","span":{"begin":26,"end":30},"obj":"SO_EXT:sequence_nullness"},{"id":"T137","span":{"begin":31,"end":37},"obj":"SO_EXT:0001023"},{"id":"T138","span":{"begin":77,"end":89},"obj":"GO:0000805"},{"id":"T139","span":{"begin":79,"end":89},"obj":"GO_SO_EXT:chromosome"},{"id":"T140","span":{"begin":117,"end":139},"obj":"UBERON:0005292"},{"id":"T141","span":{"begin":177,"end":184},"obj":"PATO_UBERON_EXT:female_or_bearer_of_femaleness"},{"id":"T142","span":{"begin":206,"end":214},"obj":"UBERON:0001987"}],"text":"e that inherit a maternal null allele should be affected, since the paternal X chromosome is normally inactivated in extraembryonic tissues. Surprisingly, however, some carrier females established a normal placenta and appeare"}

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