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Cytogenetic and Genome Research, ISSN 1424-8581, 2018, Volume 156, Issue 1, pp. 5 - 8
The aim of this study was to investigate the origin of the biallelic trisomic amplification pattern of the X chromosome microsatellite marker DXS1187 in an... 
DIAGNOSIS | Prenatal diagnosis | GENETICS & HEREDITY | Triplication | Xq26.2 | QF-PCR | CELL BIOLOGY
Journal Article
Majallah-i dānishgāh-i ̒ulūm-i pizishkī-i Arāk, ISSN 1735-5338, 11/2016, Volume 19, Issue 8, pp. 16 - 25
Abstract Background: Hydatidiform Mole is a benign trophoblastic tumor is made of ectopic preg-nancy. Abnormalities in the number or structure of chromosomes... 
Chromosomal disorders | Hydatidiform mole | QF-PCR
Journal Article
Ceska Gynekologie, ISSN 1210-7832, 06/2015, Volume 80, Issue 3, pp. 176 - 180
Journal Article
SCIENTIFIC REPORTS, ISSN 2045-2322, 05/2019, Volume 9, Issue 1, pp. 7452 - 9
Prenatal diagnosis (PND) may be complicated with sample mix-up; maternal cell contamination, non-paternity and allele drop out at different stages of... 
POPULATION | GENETIC-ANALYSIS | IRAN | MULTIDISCIPLINARY SCIENCES | PREVENTION | MUTATIONS | PROGRAM | PRENATAL-DIAGNOSIS | QF-PCR | Authenticity | Blastomeres | Trisomy | Prenatal diagnosis | Fetuses | Aneuploidy | Thalassemia | Paternity | Contamination | Genetic screening | Heterozygosity | Linkage analysis
Journal Article
Journal of Perinatal Medicine, ISSN 0300-5577, 08/2019, Volume 47, Issue 6, pp. 631 - 636
Background: Quantitative fluorescent polymerase chain reaction (QF-PCR) technique is a rapid prenatal aneuploidy detection method. This method can diagnose... 
abnormal karyotype | prenatal screening | PCR | DIAGNOSIS | PEDIATRICS | QF-PCR | OBSTETRICS & GYNECOLOGY
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2019, Volume 1885, pp. 139 - 160
Autosomal chromosome aneuploid pregnancies that survive to term, namely, trisomies 13, 18, and 21, account for 89% of chromosome abnormalities with a severe... 
Rapid prenatal test | Down syndrome | Chromosome aneuploidies | Quantitative fluorescence-polymerase chain reaction (QF-PCR)
Journal Article
CYTOGENETIC AND GENOME RESEARCH, ISSN 1424-8581, 09/2019, Volume 158, Issue 4, pp. 171 - 183
Embryonic chromosome abnormalities are the most important causes of early spontaneous abortions. The aim of this study was to evaluate the spectrum and the... 
CONCEPTION | DIAGNOSIS | 1ST-TRIMESTER | GENETIC-ANALYSIS | SPONTANEOUS-ABORTIONS | Aneuploidy | QF-PCR | CYTOGENETIC ANALYSIS | CELL BIOLOGY | PRODUCTS | Karyotyping | GENETICS & HEREDITY | Cytogenetics | Chromosome aberration | Miscarriage | COMPARATIVE GENOMIC HYBRIDIZATION | CHORIONIC VILLI | ANEUPLOIDIES
Journal Article
Hepatology, ISSN 0270-9139, 08/2007, Volume 46, Issue 2, pp. 456 - 462
Recent work has demonstrated enhanced X monosomy in women with primary biliary cirrhosis (PBC) as well as two other female‐predominant autoimmune diseases,... 
FEMALE PREDISPOSITION | WOMEN | GENE | PREGNANCIES | AUTOIMMUNITY | TURNERS-SYNDROME | IDENTIFICATION | GASTROENTEROLOGY & HEPATOLOGY | PRENATAL-DIAGNOSIS | BLOOD-CELLS | QF-PCR | Chromosomes, Human, X | Humans | Middle Aged | Chromosome Aberrations | Aged, 80 and over | Adult | Female | Male | Aged | Liver Cirrhosis, Biliary - genetics | Microsatellite Repeats
Journal Article
04/2011
Objective: G-Banding followed by standard chromosome analysis is routinely used for prenatal detection of chromosomal abnormalities. In recent years, molecular... 
Short Tandem Repeats | Chromosomal Aberration | Prenatal Diagnosis | QF-PCR
Web Resource
Reproductive Toxicology, ISSN 0890-6238, 08/2018, Volume 79, pp. 1 - 7
Trisomy 21 is a genetic condition caused when chromosomes fail to separate during meiosis We have studied conventional karyotype and QF-PCR using STR markers... 
Halt phase | Maternal meiosis-II | Down syndrome | Oocyte | QF-PCR | RECOMBINATION | MEIOTIC STAGE | RISK | BIRTH-DEFECTS | PESTICIDES | LOW SOCIOECONOMIC-STATUS | REPRODUCTIVE BIOLOGY | DOWN-SYNDROME | TOXICOLOGY | CHROMOSOME-21 | ASSOCIATION | AGE | Parenting | Genetic research | Chromosomes | Analysis
Journal Article
Acta Informatica Medica, ISSN 0353-8109, 2014, Volume 22, Issue 2, pp. 86 - 88
QF PCR has recently entered diagnostic practice as a possible way to bypass culturing of the fetal cells, as well as to provide a rapid response following... 
Kayotyping | Amniocentesis | QF PCR | Original Paper | kayotyping | amniocentesis
Journal Article
Russian Journal of Genetics, ISSN 1022-7954, 10/2019, Volume 55, Issue 10, pp. 1259 - 1265
Most common reasons for pregnancy loss are chromosomal anomalies of the fetus. They are found in as much as half of the miscarriages. The standard technique... 
Human Genetics | Biomedicine | MLPA | miscarriage | Microbial Genetics and Genomics | chromosomal aberrations | maternal cell contamination | Animal Genetics and Genomics | QF-PCR | Medical colleges | Chromosomes | Abortion | Genetic screening | Methods
Journal Article
Trends in Genetics, ISSN 0168-9525, 2012, Volume 29, Issue 2, pp. 84 - 91
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 12/2012, Volume 32, Issue 12, pp. 1197 - 1204
Objective To present the results of 10 years of quantitative fluorescence PCR (QF-PCR) analysis of prenatal samples for the rapid diagnosis of the common... 
BACS-ON-BEADS(TM) | STAND-ALONE TEST | PROBE AMPLIFICATION MLPA | DNA | GENETICS & HEREDITY | LIGATION | VILLI | EXPERIENCE | HYBRIDIZATION | CHROMOSOMAL ANEUPLOIDIES | QF-PCR | OBSTETRICS & GYNECOLOGY
Journal Article
Clinical Case Reports, ISSN 2050-0904, 01/2018, Volume 6, Issue 1, pp. 179 - 184
Key Clinical Message 48, XYYY syndrome is a rare condition. A male with 32‐year‐old and three Y chromosomes is described. This syndrome is phenotypically... 
chromosomal abnormality | QF‐PCR | 48, XYYY syndrome | sex chromosome | cytogenetic
Journal Article
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