Tissue sampling technique affects accuracy of karyotype from missed abortions

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Tissue sampling technique affects accuracy of karyotype from missed abortions is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1020591493
P356DOI10.1023/A:1020916003666
P932PMC publication ID3455340
P698PubMed publication ID12484496

P2093author name stringAmin A Milki
Ruth B Lathi
P2860cites workComparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortionsQ34390368
Cytogenetic diagnosis of "normal 46,XX" karyotypes in spontaneous abortions frequently may be misleadingQ38469392
Microsatellite analysis reveals a high incidence of maternal cell contamination in 46,XX products of conception consisting of villi or a combination of villi and membranous materialQ40693705
Frequency of abnormal karyotypes among abortuses from women with and without a history of recurrent spontaneous abortion.Q46386419
Immunological testing and treatment in reproduction: frequency assessment of practice patterns at assisted reproduction clinics in the USA and Australia.Q50683637
Karyotype of the abortus in recurrent miscarriageQ61836356
Embryonic karyotype of abortuses in relation to the number of previous miscarriagesQ73470866
P433issue11
P921main subjectabortionQ8452
karyotypeQ189967
P304page(s)536-538
P577publication date2002-11-01
P1433published inJournal of Assisted Reproduction and GeneticsQ15755113
P1476titleTissue sampling technique affects accuracy of karyotype from missed abortions
P478volume19

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cites work (P2860)
Q47631941A Yolk Sac Larger Than 5 mm Suggests an Abnormal Fetal Karyotype, Whereas an Absent Embryo Indicates a Normal Fetal Karyotype.
Q47917150A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimens
Q35115099A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing
Q33726697Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory
Q34370284Application of touch FISH in the study of mosaic tetraploidy and maternal cell contamination in pregnancy losses
Q34167161Changes in reactive oxygen species, superoxide dismutase, and hypoxia-inducible factor-1α levels in missed abortion
Q34037142Chromosome distribution of early miscarriages with present or absent embryos: female predominance
Q53664232Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study.
Q38822587Correlation between chromosomal distribution and embryonic findings on ultrasound in early pregnancy loss after IVF-embryo transfer
Q37037506Cytogenetic analysis of spontaneously discharged products of conception by array-based comparative genomic hybridization.
Q36268746Cytogenetic testing of anembryonic pregnancies compared to embryonic missed abortions
Q89447898Detecting trisomy in products of conception from first-trimester spontaneous miscarriages by next-generation sequencing (NGS)
Q89475209Early pregnancy ultrasound measurements and prediction of first trimester pregnancy loss: A logistic model
Q39032595First trimester pregnancy loss: Clinical implications of genetic testing.
Q50944086First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification.
Q35164281Genetic considerations in recurrent pregnancy loss
Q37692453Incidence of the 22q11.2 deletion in a large cohort of miscarriage samples
Q28731536Informatics enhanced SNP microarray analysis of 30 miscarriage samples compared to routine cytogenetics
Q45984200Ovarian stimulation and the risk of aneuploid conceptions
Q33788120The chromosome analysis of the miscarriage tissue. Miscarried embryo/fetal crown rump length (CRL) measurement: A practical use.

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