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European Journal of Human Genetics : EJHG
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January 2, 2022
Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype-phenotype correlations
Mateja Smogavec, Maria Gerykova Bujalkova, Reinhard Lehner, et al.
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of 2
Search research articles
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Showing results (11-20 of 11) with videos related to
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European Journal of Human Genetics : EJHG
|
January 2, 2022
Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype-phenotype correlations
Mateja Smogavec, Maria Gerykova Bujalkova, Reinhard Lehner, et al.
Page
of 2