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VAN DEN VEYVER, IGNATIA

One or more keywords matched the following items that are connected to VAN DEN VEYVER, IGNATIA

Item Type	Name
Academic Article	Single-cell analysis of the RhD blood type for use in preimplantation diagnosis in the prevention of severe hemolytic disease of the newborn.
Academic Article	Molecular analysis of human platelet antigen system 1 antigen on single cells can be applied to preimplantation genetic diagnosis for prevention of alloimmune thrombocytopenia.
Academic Article	Applied molecular genetic techniques for prenatal diagnosis.
Academic Article	Prenatal diagnosis of the RhD fetal blood type on amniotic fluid by polymerase chain reaction.
Academic Article	Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders?
Academic Article	Pheochromocytoma and Von Hippel-Lindau in pregnancy.
Academic Article	Multiplex ligation-dependent probe amplification (MLPA) and prenatal diagnosis.
Academic Article	Detection of =1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays.
Academic Article	Copy-number changes in prenatal diagnosis.
Academic Article	Preimplantation single cell analyses of dystrophin gene deletions using whole genome amplification.
Academic Article	Prenatal diagnosis and clinical findings in a case of hexasomy 12p.
Academic Article	Detection of intrauterine viral infection using the polymerase chain reaction.
Academic Article	Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy.
Academic Article	Comparative genomic hybridization and prenatal diagnosis.
Academic Article	Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.
Academic Article	Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
Academic Article	Applications of array comparative genomic hybridization in obstetrics.
Concept	Prenatal Diagnosis
Concept	Diagnosis, Differential
Concept	Preimplantation Diagnosis
Academic Article	Current controversies in prenatal diagnosis 2: should incidental findings arising from prenatal testing always be reported to patients?
Academic Article	New technologies for the assessment of chromosomes in prenatal diagnosis.
Academic Article	Noninvasive prenatal screening by next-generation sequencing.
Academic Article	Do recent US Supreme Court rulings on patenting of genes and genetic diagnostics affect the practice of genetic screening and diagnosis in prenatal and reproductive care?
Academic Article	Prenatal diagnosis of CLOVES syndrome confirmed by detection of a mosaic PIK3CA mutation in cultured amniocytes.
Academic Article	Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis.
Academic Article	Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.
Academic Article	Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice.
Academic Article	Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women.
Academic Article	Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Academic Article	Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
Academic Article	The uptake of pan-ethnic expanded carrier screening is higher when offered during preconception or early prenatal genetic counseling.
Academic Article	Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Grant	New strategies to identify the gene mutated in Aicardi syndrome
Grant	Prenatal Genetic Diagnosis by Genomic Sequencing: A Prospective Evaluation
Grant	Baylor Intellectual and Developmental Disabilities Research Center
Grant	FUNCTIONAL ANALYSIS OF CANDIDATE GENES FOR MLS SYNDROME
Academic Article	Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing.
Academic Article	Prenatally diagnosed developmental abnormalities of the central nervous system and genetic syndromes: A practical review.
Academic Article	Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis.
Academic Article	Current controversies in prenatal diagnosis 2: The 59 genes ACMG recommends reporting as secondary findings when sequencing postnatally should be reported when detected on fetal (and parental) sequencing.
Academic Article	Prenatal testing in pregnancies conceived by in vitro fertilization with pre-implantation genetic testing.
Academic Article	Improving the prenatal diagnosis of Beckwith-Wiedemann syndrome.
Academic Article	International Society for Prenatal Diagnosis Updated Position Statement on the use of genome-wide sequencing for prenatal diagnosis.
Academic Article	Lack of consensus among healthcare professionals at a large academic medical center on the use of exome sequencing for prenatal diagnosis.
Academic Article	Implication of chromosomal microarray analysis prior to in-utero repair of fetal open neural tube defect.
Academic Article	Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series.
Academic Article	Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis.
Academic Article	International Society for Prenatal Diagnosis 2022 debate 3-Fetal genome sequencing should be offered to all pregnant patients.
Academic Article	Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants.

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Diagnosis