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UnknownA prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound.
Not available
S-EPMC7540374 | biostudies-literature
UnknownEvidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.
Not available
S-EPMC5589990 | biostudies-literature
UnknownMonoallelic NTHL1 Loss-of-Function Variants and Risk of Polyposis and Colorectal Cancer.
Not available
S-EPMC7899696 | biostudies-literature
UnknownRisk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.
Not available
S-EPMC8026395 | biostudies-literature
UnknownCancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.
Not available
S-EPMC7371626 | biostudies-literature
UnknownUptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.
Not available
S-EPMC8916840 | biostudies-literature
UnknownNo Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study.
Not available
S-EPMC8269121 | biostudies-literature
UnknownVariation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study.
Not available
S-EPMC8934577 | biostudies-literature
UnknownOutcomes of elective liver surgery worldwide: a global, prospective, multicenter, cross-sectional study.
Not available
S-EPMC10720814 | biostudies-literature
UnknownImpact of the COVID-19 pandemic on surgical care in the Netherlands.
Not available
S-EPMC10364688 | biostudies-literature
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