Aiming at multidisciplinary consensus: what should be detected in prenatal diagnosis?
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference15 articles.
1. Comparison of multiplex ligation-dependent probe amplification and karyotyping in prenatal diagnosis;Boormans;Obstet Gynecol,2010
2. Multiplex ligation-dependent probe amplification versus karyotyping in prenatal diagnosis: the MA.K.E. study;Boormans;BMC Pregnancy Childbirth,2008
3. Prenatal cytogenetic diagnosis: gone FISHing, BAC soon!;Bui;Ultrasound Obstet Gynecol,2007
4. Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment;Caine;Lancet,2005
5. Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR, results of 9 years of clinical experience;Cirigliano;Prenat Diagn,2009
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2. Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross‐sectional study with healthcare professionals;Prenatal Diagnosis;2021-03-30
3. Detection of copy number variants with chromosomal microarray in 10 377 pregnancies at a single laboratory;Acta Obstetricia et Gynecologica Scandinavica;2020-05-17
4. Maternity health care professionals' views and experiences of fetal genomic uncertainty: A review;Prenatal Diagnosis;2020-04-20
5. Pregnancy outcomes in 188 French cases of prenatally diagnosed Klinefelter syndrome;Human Reproduction;2011-07-05
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