Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US. Read more about Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US.
Investigating attitudes toward prenatal diagnosis and fetal therapy for spinal muscular atrophy. Read more about Investigating attitudes toward prenatal diagnosis and fetal therapy for spinal muscular atrophy.
Challenges in providing residual risks in carrier testing. Read more about Challenges in providing residual risks in carrier testing.
Preference for secondary findings in prenatal and pediatric exome sequencing. Read more about Preference for secondary findings in prenatal and pediatric exome sequencing.
Cytogenetic signatures of recurrent pregnancy losses. Read more about Cytogenetic signatures of recurrent pregnancy losses.
False negative fetal cell free DNA screening for microdeletion syndromes in the presence of an unbalanced translocation involving monosomy 4p. Read more about False negative fetal cell free DNA screening for microdeletion syndromes in the presence of an unbalanced translocation involving monosomy 4p.
Placental transcriptomes in the common aneuploidies reveal critical regions on the trisomic chromosomes and genome-wide effects. Read more about Placental transcriptomes in the common aneuploidies reveal critical regions on the trisomic chromosomes and genome-wide effects.
False positive cell free DNA screening for microdeletions due to non-pathogenic copy number variants. Read more about False positive cell free DNA screening for microdeletions due to non-pathogenic copy number variants.
Prenatal whole-exome sequencing: parental attitudes. Read more about Prenatal whole-exome sequencing: parental attitudes.
High resolution non-invasive detection of a fetal microdeletion using the GCREM algorithm. Read more about High resolution non-invasive detection of a fetal microdeletion using the GCREM algorithm.
