Amniocentesis and chorionic villus sampling.

No abstract is available for this paper.

• Publication year

  1993

• Venue

  Western Journal of Medicine

• Publication date

  Unknown publication date

• Fields of study

  Medicine

• Identifiers
  PMID 8236967PMCID PMC1011338
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Procedure-related fetal losses in transplacental versus nontransplacental genetic amniocentesis.

  1995cited by this paper
• Transplacental amniocentesis: Is it really a higher‐risk procedure?

  1994cited by this paper
• Comparison of chorionic villus sampling and amniocentesis for fetal karyotyping at 10-13 weeks' gestation.

  1994cited by this paper
• Randomized comparison of amniocentesis and transabdominal and transcervical chorionic villus sampling

  1993cited by this paper
• Amniocentesis and Its Complications

  1992cited by this paper
• Early amniocentesis: outcome, risks, and technical problems at less than or equal to 12.8 weeks.

  1992cited by this paper
• Early amniocentesis.

  1992cited by this paper
• Early amniocentesis: Outcome, risks, and technical problems at ≤ 12.8 weeks

  1992cited by this paper
• Limb Anomalies Associated With Chorionic Villus Sampling

  1992cited by this paper
• A randomized comparison of transcervical and transabdominal chorionic-villus sampling. The U.S. National Institute of Child Health and Human Development Chorionic-Villus Sampling and Amniocentesis Study Group.

  1992cited by this paper
• Cytogenetic results from the U.S. collaborative study on CVS

  1992cited by this paper
• Transvaginal chorionic villus sampling using transabdominal ultrasound guidance

  1992cited by this paper
• Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation.

  1991cited by this paper
• Direct analysis of uncultured cytotrophoblastic cells from second‐ and third‐trimester placentas: An accurate and rapid method for detection of fetal chromosome abnormalities

  1991cited by this paper
• Prenatal diagnosis in multiple gestation: 20 Years' experience with amniocentesis

  1991cited by this paper
• Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation

  1991cited by this paper
• Randomized clinical trial of transabdominal versus transcervical chorionic villus sampling methods

  1991cited by this paper
• Early amniocentesis: alphafetoprotein levels in amniotic fluid, extraembryonic coelomic fluid and maternal serum between 8 and 13 weeks

  1991cited by this paper
• An assessment of hazards of amniocentesis

  1990cited by this paper
• Early amniocentesis: Experience of 222 consecutive patients, 1987–1988

  1990cited by this paper
• [Early amniocentesis].

  1990cited by this paper
• Audit of amniocentesis from a district general hospital: is it worth it?

  1990cited by this paper
• Early amniocentesis.

  1990cited by this paper
• The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities.

  1989cited by this paper
• Transabdominal chorionic villus sampling for first-trimester prenatal diagnosis.

  1989cited by this paper
• MULTICENTRE RANDOMISED CLINICAL TRIAL OF CHORION VILLUS SAMPLING AND AMNIOCENTESIS First Report

  1989cited by this paper
• Limb reduction defects in over one million consecutive livebirths.

  1989cited by this paper
• False‐Positive Acetylcholinesterase With Early Amniocentesis

  1989cited by this paper
• Rapid karyotyping for prenatal diagnosis in the second and third trimesters of pregnancy

  1988cited by this paper
• Transabdominal versus transcervical chorionic villus sampling: a randomized trial.

  1988cited by this paper
• Early amniocentesis for prenatal cytogenetic evaluation.

  1988cited by this paper
• Early amniocentesis and amniotic fluid AFP levels.

  1987cited by this paper
• Safety of placental biopsy in the second and third trimesters.

  1987cited by this paper
• Low fetal loss rates after ultrasound-proved viability in early pregnancy.

  1987cited by this paper
• Amniocentesis: a Comparison of ‘Monitored’ versus ‘Blind’ Needle Insertion Technique

  1986cited by this paper
• Randomised controlled trial of genetic amniocentesis in 4606 low-risk women.

  1986influential reference
• Sonographically monitored amniocentesis to decrease intraoperative complications.

  1985cited by this paper
• Risks of midtrimester amniocentesis; assessment in 3000 pregnancies

  1985cited by this paper
• Reduction in amniocentesis risks using a real-time needle guide procedure.

  1985cited by this paper
• Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis

  1984cited by this paper
• United states survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis

  1984cited by this paper
• Hypermodal cells in amniotic fluid cultures: frequency, interpretation, and clinical significance.

  1982cited by this paper
• Genetic amniocentesis in twin gestations.

  1980cited by this paper
• AMNIOCENTESIS WITH AND WITHOUT ULTRASOUND GUIDANCE

  1979cited by this paper
• Prenatal diagnosis of genetic disorders.

  1978cited by this paper

• Application of Chorionic Villus Sampling to Longitudinal Studies in Pregnant Non-Human Primate Models

  2026cites this paper
• A Four-Year Retrospective Study of Amniocentesis in a Tertiary Care Center in South India—Lessons Learnt

  2025cites this paper
• Current Approaches to Prenatal Diagnosis of Sickle Cell Anaemia

  2025cites this paper
• Construction and Evaluation of a Ballistic Gelatin-Based Simulator for Transcervical Chorionic Villus Sampling.

  2025cites this paper
• Comparison of pregnancy outcomes in amniocentesis recipients with normal and abnormal maternal serum analytes.

  2024cites this paper
• The association of prenatal amniotic sex hormones and digit ratio (2D:4D) in children aged 5 to 70 months: A longitudinal study

  2023cites this paper
• Empfehlungen der DEGUM zu diagnostischen Punktionen in der Pränatalmedizin DEGUM Recommendations on Diagnostic Puncture in Prenatal Medicine

  2023cites this paper
• Empfehlungen der DEGUM zu diagnostischen Punktionen in der Pränatalmedizin

  2022cites this paper
• Expert Perspectives on the Management of Alpha 1-Antitrypsin Deficiency.

  2022cites this paper
• Foetal loss after chorionic villus sampling and amniocentesis in twin pregnancies: A multicentre retrospective cohort study

  2022cites this paper
• Data-Driven Medicine in the Diagnosis and Treatment of Infertility

  2022cites this paper
• Invasive Prenatal Diagnostic Testing for Aneuploidies in Singleton Pregnancies: A Comparative Review of Major Guidelines

  2022cites this paper
• Difference in Procedure-Related Risk of Miscarriage between Early and Mid-Trimester Amniocentesis: A Retrospective Cohort Study

  2021cites this paper
• Evaluation of short-term safety of ultrasound-guided foetal fluid sampling in the dog (Canis lupus familiaris).

  2021cites this paper
• Outcome of antenatal invasive diagnostic tests in a fetal medicine unit with low case load in North Wales, United Kingdom

  2021cites this paper
• Fetal information as shared information: using NIPT to test for adult-onset conditions

  2021cites this paper
• Comparison of indications and results of prenatal invasive diagnostic tests before and after the implementation of the use of cell-free fetal DNA: a tertiary referral center experience

  2020cites this paper
• Prenatal Diagnosis in Sickle Cell Disease: In the Eyes of the Couple at Risk

  2020cites this paper
• Big Data and Artificial Intelligence (AI) are Poised to Transform Infertility Healthcare

  2020cites this paper
• Fetal and maternal safety considerations for in utero therapy clinical trials: iFeTiS consensus statement.

  2020cites this paper
• Prenatal screening and diagnosis of genetic abnormalities: SEGO, SEQCML, AEDP consensus recommendations

  2020cites this paper
• Genetic Disorders in the Fetus from Diagnosis to Treatment

  2020influential citation
• Pregnancy Loss After Amniocentesis and Chorionic Villus Sampling: Cohort Study

  2020cites this paper
• False-Positive Results in Pregnancy Screening for Aneuploidy

  2020cites this paper
• 5-Fetal Physiology

  2019cites this paper
• Antenatal care

  2019cites this paper
• Congenital Malformations: Prenatal Diagnosis and Management

  2019cites this paper
• Trials and tribulations of meta‐analyzing procedure‐related risks of amniocentesis and chorionic villus sampling

  2019cites this paper
• Molecular Techniques for Prenatal Diagnosis

  2019cites this paper
• Cerclage outcome by the type of suture material (COTS) study: randomised pilot/feasibility study comparing monofilament (intervention) sutures versus multifilament (comparison) for cervical cerclage

  2018cites this paper
• Cross-cultural perspectives on decision making regarding noninvasive prenatal testing: A comparative study of Lebanon and Quebec

  2018influential citation
• Functional analysis of cell-free RNA using mid-trimester amniotic fluid supernatant in pregnancy with the fetal growth restriction

  2018cites this paper
• Early prenatal screening in Iceland and Norway - Background and current situation

  2017cites this paper
• Women's decision making process regarding prenatal diagnostic testing

  2017cites this paper
• Chorionic Villus Sampling

  2016cites this paper
• Comparative Value of Real Time and Conventional PCR in Antenatal Gender Determination

  2016cites this paper
• How to safeguard competency and training in invasive prenatal diagnosis: ‘the elephant in the room’

  2016cites this paper
• Transcervical chorionic villus sampling: a practical guide

  2016cites this paper
• ISUOG Practice Guidelines: invasive procedures for prenatal diagnosis

  2016cites this paper
• Genetic Ultrasound Scan—Second Trimester

  2016cites this paper
• Sonographic soft markers in the second trimester: Subtle indicators or significant findings?

  2015cites this paper
• Emerging issues in invasive prenatal diagnosis: Safety and competency in the post‐NIPT era

  2015cites this paper
• Will the introduction of non‐invasive prenatal testing for Down's syndrome undermine informed choice?

  2015cites this paper
• Invasive prenatal testing at a Tertiary Fetal Medicine referral center in Sri Lanka: A service evaluation audit

  2015cites this paper
• Neinvazivno predrojstveno testiranje proste plodove DNA za downov sindrom in ostale kromosomske nepravilnosti

  2015cites this paper
• Variation in expression of fetal nucleic acids in maternal blood in pregnancies affected by congenital anomalies

  2015cites this paper
• Alpha fetoprotein and ultrasound in the prenatal diagnosis

  2015cites this paper
• Overview of the impact of noninvasive prenatal testing on diagnostic procedures

  2015cites this paper
• Chorionic villus sampling for early prenatal diagnosis: Experience at a mainland Chinese hospital

  2014cites this paper
• A historical and practical review of first trimester aneuploidy screening.

  2014cites this paper
• Prenatal Molecular Diagnosis of β-Thalassemia and Sickle Cell Anemia in the Syrian Population

  2014cites this paper
• A national perspective on prenatal testing for mitochondrial disease

  2014cites this paper
• Fósturlát í kjölfar legvatnsástungu og fylgjusýnitöku á Íslandi

  2014cites this paper
• Early fetal gender determination using real-time PCR analysis of cell-free fetal DNA during 6th-10th weeks of gestation.

  2013cites this paper
• [DEGUM guidelines for amniocentesis and chorionic villus sampling].

  2013cites this paper
• Empfehlungen der DEGUM zur Durchführung von Amniozentese und Chorionzottenbiopsie

  2013cites this paper
• Micro-scale blood plasma separation: from acoustophoresis to egg-beaters.

  2013cites this paper
• Set Adrift in the Prenatal Diagnostic Marketplace: Analyzing the Role of Users and Mediators in the History of a Medical Technology

  2013cites this paper
• Improved first‐trimester aneuploidy risk assessment: an evolving challenge of training in invasive prenatal diagnosis

  2013cites this paper
• Just prenatal testing? The science, ethics, and policy of testing for Down syndrome

  2013cites this paper
• Implementing non-invasive RHD genotyping on cell-free foetal DNA from maternal plasma: the Pavia experience.

  2012cites this paper
• Optimal cut‐offs for down syndrome contingent screening in a population of 10 156 pregnant women

  2012cites this paper
• Informing on prenatal screening for Down syndrome prior to conception. An empirical and ethical perspective

  2012cites this paper
• Pregnancy loss after chorionic villus sampling and genetic amniocentesis in twin pregnancies: a systematic review

  2012cites this paper
• Large-Scale Pre-Diagnosis Study of Fetal RHD Genotyping by PCR on Plasma DNA from RhD-Negative Pregnant Women

  2012cites this paper
• Non-invasive prenatal diagnostics of aneuploidy using next-generation DNA sequencing technologies, and clinical considerations

  2012cites this paper
• Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases

  2011cites this paper
• Guideline on the management of haemophilia in the fetus and neonate *

  2011cites this paper
• Comparison of Two National Guidelines in Obstetrics: American versus Royal College of Obstetricians and Gynecologists

  2010cites this paper
• Current and emerging techniques of fetal cell separation from maternal blood.

  2010cites this paper
• Noninvasive prenatal diagnosis of fetal blood group phenotypes: current practice and future prospects

  2009cites this paper
• Ductus Venosus Pulsatility Index as an Antenatal Screening Marker for Down'S Syndrome: Use with the Combined and Integrated Tests

  2009cites this paper
• Procedimientos invasivos intrauterinos

  2009cites this paper
• Update on Procedure-Related Risks for Prenatal Diagnosis Techniques

  2009cites this paper
• ANALYSIS OF POLYCYCLIC AROMATIC HYDROCARBONS IN AMNIOTIC FLUID SAMPLES FROM SMOKERS AND NONSMOKERS

  2008cites this paper
• Prenatal diagnosis of cystic fibrosis: the 18‐year experience of Brittany (western France)

  2008cites this paper
• Monitoring obstetricians’ performance with statistical process control charts

  2007cites this paper
• The obstetric and gynaecological management of women with inherited bleeding disorders – review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors’ Organization

  2006cites this paper
• Sequential and contingent prenatal screening for Down syndrome

  2006cites this paper
• Amniotic Fluid: Not Just Fetal Urine Anymore

  2005cites this paper
• Characterization of the human CD34+ hematopoietic progenitor cell compartment during the second trimester of pregnancy.

  2005cites this paper
• SURUSS in perspective

  2004cites this paper
• Fetal blood group genotyping from DNA from maternal plasma: an important advance in the management and prevention of haemolytic disease of the fetus and newborn

  2004cites this paper
• A report of early (13 + 0 to 14 + 6 weeks) and mid-trimester amniocenteses: 10 years' experience

  2003cites this paper
• First and Second Trimester Antenatal Screening for Down's Syndrome: The Results of the Serum, Urine and Ultrasound Screening Study (SURUSS)

  2003cites this paper
• Cytogenetics and molecular cytogenetics in prenatal diagnosis.

  2003cites this paper
• Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping service

  2002cites this paper
• Prenatal diagnosis of the Wiskott–Aldrich syndrome by PCR‐based methods

  2001cites this paper
• Prenatal diagnosis of congenital anomalies

  2001cites this paper
• Trends in the use of prenatal diagnosis in New York State and the impact of biochemical screening on the detection of Down syndrome: 1984–1993

  1997cites this paper
• Transabdominale Chorionzotten-und Plazentabiopsie: Rasche Karyotypisierung im 1.-3. Trimenon der Schwangerschaft

  1997cites this paper
• Treatment of X-linked severe combined immunodeficiency by in utero transplantation of paternal bone marrow.

  1996cites this paper
• Pathologic examination of fetal specimens from dilation and evacuation procedures.

  1995cites this paper
• Advances in the prenatal and molecular diagnosis of the hemoglobinopathies and thalassemias.

  1995cites this paper
• Prenatally detected fetal myelomeningocele: is karyotype analysis warranted?

  1995cites this paper
• Isolated mild fetal cerebral ventriculomegaly: clinical course and outcome.

  1994cites this paper