Credibility of the combined test in prenatal diagnostics (original) (raw)

Value of the Combined Test in Prenatal Diagnostics

Balkan Journal of Medical Genetics, 2010

Evaluation of Invasive Prenatal Test Indications and Results at a Tertiary Center in the Thrace Region of Turkey

Journal of Clinical Obstetrics & Gynecology, 2019

One stop clinic for assessment of risk for fetal anomalies: a report of the first year of prospective screening for chromosomal anomalies in the first trimester

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BJOG: An International Journal of Obstetrics and Gynaecology, 2000

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Screening for chromosomal anomalies: first or second trimester, biochemical or ultrasound?

Taita Stojilkovic

Annals of the Academy of Medicine, Singapore, 2003

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Contribution of “modified genetic sonography” to the combined test as a screening method for chromosomal abnormalities

Rogelio Garrido

The Journal of Maternal-Fetal & Neonatal Medicine, 2011

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Screening for fetal chromosomal abnormalities by maternal serum biochemistry and ultrasound examination of fetal morphology

Recep Has

Current Opinion in Obstetrics and Gynecology, 1993

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The Reliability of Maternal Serum Triple Test in Prenatal Diagnosis of Fetal Chromosomal Abnormalities of Pregnant Turkish Women

Osman Demirhan

Genetic Testing and Molecular Biomarkers, 2011

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Advanced first trimester screening (AFS): an improved test strategy for the individual risk assessment of fetal aneuploidies and malformations

Alexander Scharf

Archives of Gynecology and Obstetrics, 2007

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Impact of Material Serum Screening in Early Prenatal Diagnosis and Management of Congenital Anomalies

Cristina-Crenguta Albu

Revista de Chimie

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Biochemical screening of fetal aneuploidies and neural tube defects by "double-test" in Croatia: a 10 years' experience

Ivan Bolanca

Collegium antropologicum, 2011

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Integrated Screening for Chromosomal Anomalies: Strategies in Developing Countries

ruchika garg

Donald School Journal of Ultrasound in Obstetrics & Gynecology, 2011

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Sensitivity and specificity of prenatal screening methods for detection of risk of fetal chromosomal abnormalities

Sunil Juneja

International Journal of Reproduction, Contraception, Obstetrics and Gynecology

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From screening chromosomal anomalies to early diagnosis of fetal malformations

LAURA ADAMO

Current Opinion in Obstetrics and Gynecology, 2020

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Assessment of a change of protocol of prenatal screening by inclusion of non-invasive prenatal diagnosis

Miguel Angel Castaño López

Advances in laboratory medicine, 2020

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Predictive Value of Fetal Nuchal Translucency in Screening of Chromosomal Aberrations

Dragan Loncar

Acta Medica Medianae, 2011

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The importance of screening and prenatal diagnosis in the identification of the numerical chromosomal abnormalities

DELIA NEAGOS

Mædica, 2011

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Testing for fetal abnormality in routine antenatal care

Josephine Green, H. Statham

Midwifery, 1993

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Sonography Markers of Chromosomal Abnormality in Second Trimester

Jayprakash Shah

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Correlation between maternal serum biochemical markers with karyotyping for prenatal screening of foetal chromosomal abnormalities

chandrashankar Gupta

International Journal of Reproduction, Contraception, Obstetrics and Gynecology, 2017

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Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly

Claudio Celentano

Prenatal Diagnosis, 2005

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Ultrasound findings before amniocentesis in selecting the method of analysing the sample

Makarios Eleftheriades

Prenatal Diagnosis, 2007

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First trimester combined screening for chromosomal defects: Our results in a population with a high percent of women aged 35 or older

Markku Ryynänen

The Ultrasound Review of Obstetrics & Gynecology, 2005

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Retrospective Evaluation of Results of 3617 Invasive Prenatal Diagnosis Cases Applied Between 1997-2015 Years

Mustafa Basbug

Sağlık bilimleri dergisi, 2016

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Changes in Clinical and Cytogenetic Findings of Invasive Prenatal Diagnosis from 1989 to 2011 in Istanbul; Impact of the Biochemical Screening Tests and Fetal Ultrasonography

Birsen Karaman

2020

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Clinical Significance of Conventional Karyotype and QF-PCR in Detection of Fetal Chromosomal Abnormalities

Amina Kurtovic, Mirsada Hukić

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Aiming at multidisciplinary consensus: what should be detected in prenatal diagnosis?

E. Birnie

Prenatal Diagnosis, 2010

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Prenatal Screening of Cytogenetic Anomalies -A Ten Year Retrospective Study on 1510 Cases

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European journal of medical and health sciences, 2023

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Early diagnosis of fetal abnormalities – the importance of ultrasonographic examination

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Romanian Medical Journal

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Credibility of the combined test in prenatal diagnostics (original) (raw)

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