Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference14 articles.
1. Cytogenetic and molecular analysis in trisomy 12p;Allen;Am. J. Med. Genet.,1996
2. Trisomy 12(pter––q12) and monosomy 21(pter––q21). A propos of a case;Arnaud;J. Genet. Hum.,1984
3. Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12;Cetin;Am. J. Med. Genet. A,2011
4. Trisomy 12p syndrome: a chromosomal disorder associated with generalized 3-Hz spike and wave discharges;Guerrini;Epilepsia,1990
5. Phenotypic overlapping of trisomy 12p and Pallister–Killian syndrome;Inage;Eur. J. Med. Genet.,2010
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1. Non-mosaic partial duplication 12p in a patient with dysmorphic characteristics and developmental delay;Genetics and Molecular Biology;2020
2. Prevalence of chromosomal abnormalities identified by copy number variation sequencing in high-risk pregnancies, spontaneous abortions, and suspected genetic disorders;Journal of International Medical Research;2019-02-07
3. Phenotype to genotype characterization by array-comparative genomic hydridization (a-CGH) in case of fetal malformations: A systematic review;Taiwanese Journal of Obstetrics and Gynecology;2019-01
4. Non-invasive prenatal detection for copy number variation;Clinical and Experimental Obstetrics & Gynecology;2018-04-10
5. Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, X, and Y using segmental duplication quantitative fluorescent PCR (SD-QF-PCR);Gene;2017-09
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