Positive non-invasive prenatal testing for trisomy 13 in the first trimester in a pregnancy with fetal holoprosencephaly, cebocephaly and postaxial polydactyly

Bibliographic Details
Main Author:	Chih-Ping Chen (Author)
Format:	Book
Published:	Elsevier, 2024-01-01T00:00:00Z.
Subjects:	article
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Prenatal Visualization of Cebocephaly with a Prominent Nose in a Second-trimester Fetus with Alobar Holoprosencephaly and Trisomy 13
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Rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction analysis in a pregnancy with fetal holoprosencephaly, premaxillary agenesis, postaxial polydactyly of left hand and overriding aorta
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Rapid confirmation of trisomy 13 of maternal origin by QF-PCR following postmortem tissue cell culture failure in a pregnancy with trisomy 13 at amniocentesis and fetal postaxial polydactyly and facial cleft
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Review on Genes related to Postaxial Polydactyly
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Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother
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Application of quantitative fluorescent polymerase chain reaction analysis for the rapid confirmation of trisomy 13 of maternal origin in a pregnancy with fetal holoprosencephaly, cyclopia, polydactyly, omphalocele and cell culture failure
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Alobar holoprosencephaly and Trisomy 13 (Patau syndrome)
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Low-level mosaic trisomy 21 at amniocentesis and cordocentesis in the second trimester in a pregnancy associated with positive non-invasive prenatal testing for trisomy 21, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome
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Prenatal Diagnosis and Genetic Counseling for Mosaic Trisomy 13
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Rapid confirmation of maternal origin of trisomy 21 by quantitative fluorescent polymerase chain reaction in a fetus associated with increased nuchal translucency, abnormal first-trimester maternal serum screening result and positive non-invasive prenatal testing for trisomy 21
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Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (IV)
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Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (I)
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Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (II)
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Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (III)
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An atypical case of Klippel-Trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report
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False positive non-invasive prenatal testing (NIPT) for trisomy 12 in a pregnancy associated with a favorable fetal outcome and normal hemogram in the pregnant woman
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Prenatal Diagnosis and Molecular Analysis of Trisomy 13 Mosaicism
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False negative non-invasive prenatal testing (NIPT) result for trisomy 7 and false positive NIPT result for trisomy 2 in a pregnancy associated with low-level mosaic trisomy 7 at amniocentesis and a favorable outcome
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Prenatal Diagnosis of Alobar Holoprosencephaly, Cyclopia, Proboscis, and Isochromosome 18q in the Second Trimester
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First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism
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Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepancy in various tissues and a favorable fetal outcome
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HOLOPROSENCEPHALY: FETAl, NEUROLOGICAL AND CLINICAL ASPECTS, PRENATAL DIAGNOSTICS, CASES FROM PRACTICE
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Mosaic trisomy 16 at amniocentesis in a pregnancy associated with positive non-invasive prenatal testing for trisomy 16, placental trisomy 16, intrauterine growth restriction, intrauterine fetal death, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, and prenatal progressive decrease of the aneuploid cell line
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Rapid diagnosis of maternal origin of fetal trisomy 13 by quantitative fluorescent polymerase chain reaction in a pregnancy associated with young maternal age and omphalocele on prenatal ultrasound
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False positive non-invasive prenatal testing (NIPT) for trisomy 21 in vanishing twin syndrome pregnancy: A comparison of the NIPT results performed in different gestations
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Low-level mosaic trisomy 9 at amniocentesis associated with a positive non-invasive prenatal testing for trisomy 9, maternal uniparental disomy 9, intrauterine growth restriction and a favorable fetal outcome in a pregnancy
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Low-level mosaic trisomy 14 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, positive non-invasive prenatal testing for trisomy 14, perinatal progressive decrease of the trisomy 14 cell line and a favorable fetal outcome
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Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism
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Placental Abnormalities and Preeclampsia in Trisomy 13 Pregnancies
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Prenatal Diagnosis of a Congenital Postaxial Longitudinal Limb Defect: A Case Report
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Prenatal Diagnosis of Alobar Holoprosencephaly with Cystic Hygroma
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Prenatal diagnosis of alobar holoprosencephaly associated with cyclopia
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High-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with positive NIPT for trisomy 21, prenatal progressive decrease of the trisomy 21 cell line, acute fatty liver of pregnancy and intrauterine fetal death in late gestation
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Rapid detection of maternal origin of trisomy 18 by quantitative fluorescent polymerase chain reaction in a fetus associated with increased nuchal translucency thickness and omphalocele on first-trimester prenatal ultrasound
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Correlation of Ultrasonography and MRI in Prenatal Diagnosis of Lobar Holoprosencephaly
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Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy
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Positive non-invasive prenatal testing for trisomy 13 in the first trimester in a pregnancy with fetal holoprosencephaly, cebocephaly and postaxial polydactyly

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