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Familial Risk of Placental Abruption
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Copy number variants and fetal structural abnormalities in stillborn fetuses: a secon...
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Whole-genome sequencing analysis in families with recurrent pregnancy loss: A pilot s...
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Familial aggregation of stillbirth: a pedigree analysis of a matched case control stu...
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Copy number variants and placental abnormalities in stillborn fetuses: a secondary an...
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