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CHEUNG, SAU WAI

One or more keywords matched the following items that are connected to CHEUNG, SAU WAI

Item Type	Name
Academic Article	First trimester chorionic villus sampling versus mid-trimester genetic amniocentesis--preliminary results of a controlled prospective trial.
Academic Article	Chromosome mosaicism and maternal cell contamination in chorionic villi.
Academic Article	An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villus versus fetal tissue.
Academic Article	A simple method for preparing prometaphase chromosomes from amniotic fluid cell cultures.
Academic Article	Antenatal ultrasound findings in fetal triploidy syndrome.
Academic Article	Exclusion of chromosomal mosaicism in amniotic fluid cultures: determination of number of colonies needed for accurate analysis.
Academic Article	Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
Academic Article	Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives.
Academic Article	The array CGH and its clinical applications.
Academic Article	Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH.
Academic Article	Exclusion of chromosomal mosaicism in amniotic fluid cultures: efficacy of in situ versus flask techniques.
Academic Article	Prenatal diagnosis of PLP1 copy number by array comparative genomic hybridization.
Academic Article	Development and validation of a CGH microarray for clinical cytogenetic diagnosis.
Academic Article	High resolution R banding in amniotic fluid cells using the BrdU-Hoechst 33258-Giemsa (RBG) technique.
Academic Article	Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.
Academic Article	Prenatal diagnosis by array-based comparative genomic hybridization in the clinical laboratory setting.
Academic Article	Molecular cytogenetic evidence to characterize breakpoint regions in Robertsonian translocations.
Academic Article	Detection of =1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays.
Academic Article	Suspected trisomy 22: Modification, clarification, or confirmation of the diagnosis by aCGH.
Academic Article	Prenatal diagnosis, fetal pathology, and cytogenetic analysis of mosaic trisomy 14.
Academic Article	Prenatal diagnosis of a fetus with a homologous Robertsonian translocation of chromosomes 15.
Academic Article	Confirmation of paternal disomy in a twin molar pregnancy. A case report.
Academic Article	Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study.
Academic Article	Sensitivity of chromosomal mosaicism detected by different tissue culture methods.
Academic Article	Evolution of prenatal genetics: from point mutation testing to chromosomal microarray analysis.
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	10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.
Concept	Prenatal Diagnosis
Concept	Diagnosis, Differential
Concept	Diagnosis
Concept	Preimplantation Diagnosis
Academic Article	Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.
Academic Article	Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics era.
Academic Article	Accurate description of DNA-based noninvasive prenatal screening.
Academic Article	Application of DNA Microarray to Clinical Diagnostics.
Academic Article	Contribution of genomic copy-number variations in prenatal oral clefts: a multicenter cohort study.
Academic Article	4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions.
Academic Article	Prenatal detection of 10q22q23 duplications: dilemmas in phenotype prediction.
Academic Article	Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
Academic Article	Clinical Reasoning: A common cause for Phelan-McDermid syndrome and neurofibromatosis type 2: One ring to bind them.
Academic Article	Prenatal diagnosis of Wolf-Hirschhorn syndrome: from ultrasound findings, diagnostic technology to genetic counseling.
Academic Article	Targeted gene panel sequencing prenatally detects two novel mutations of DYNC2H1 in a fetus with increased biparietal diameter and polyhydramnios.
Academic Article	Microarray analysis: First-trimester maternal serum free ?-hCG and the risk of significant copy number variants.
Academic Article	Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1-2 (BP1-BP2) in a large cohort of samples referred for genetic diagnosis.
Academic Article	Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases.
Academic Article	Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.
Academic Article	Noninvasive prenatal screening for fetal sex chromosome aneuploidies.

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Diagnosis