Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype–phenotype correlations - Concepedia

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Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype–phenotype correlations

DOI Full Paper Access

12

Citations

33

References

2022

Year

Mateja Smogavec, Maria Gerykova Bujalkova, Reinhard Lehner, Jürgen Neesen, Jana Behunova, Gülen Yerlikaya‐Schatten, Theresa Reischer, R Altmann, Denisa Weis, Hans‐Christoph Duba,

European Journal of Human Genetics

References

	Year	Citations

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