Works matching DE "CHORIONIC villus sampling"

Results: 715

Dijagnostički prinos kromosomskog mikropostroja u prenatalnom otkrivanju genomskih poremećaja.

Published in:

Paediatria Croatica, 2025, v. 69, p. 97, doi. 10.13112/pc.1056

By:

Stipoljev, Feodora;
Oroz, Maja;
Hafner, Tomislav;
Vlatković, Ivanka Bekavac;
Zudenigo, Damir;
Matijević, Ratko;
Vuk, Tamara;
Mustapić, Ana

Publication type:

Article

Fetal karyotyping in adolescent pregnancies: a population-based cohort study on outcomes of invasive prenatal testing.

Published in:

Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1581249

By:

Staniczek, Jakub;
Manasar-Dyrbuś, Maisa;
Sodowska, Patrycja;
Sodowski, Krzysztof;
Włoch, Agata;
Czuba, Bartosz;
Cnota, Wojciech;
Paul-Samojedny, Monika;
Kania, Agnieszka;
Sodowska, Henryka;
Rybak-Krzyszkowska, Magda;
Kondracka, Adrianna;
Stojko, Rafał;
Drosdzol-Cop, Agnieszka

Publication type:

Article

Declining invasive prenatal diagnostic procedures: A comparison of tertiary hospital and national data from 2012 to 2015.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 2017, v. 57, n. 2, p. 152, doi. 10.1111/ajo.12590

By:

Johnson, Kristine;
Kelley, Joanne;
Saxton, Virginia;
Walker, Susan P.;
Hui, Lisa

Publication type:

Article

Emerging issues in invasive prenatal diagnosis: Safety and competency in the post-NIPT era.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 2015, v. 55, n. 6, p. 541, doi. 10.1111/ajo.12396

By:

Hui, Lisa;
The, Stephanie;
McCarthy, Elizabeth A.;
Walker, Susan P.

Publication type:

Article

The selective use of rapid aneuploidy screening in prenatal diagnosis.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 2009, v. 49, n. 1, p. 28, doi. 10.1111/j.1479-828X.2008.00939.x

By:

Dickinson, Jan E.;
Harcourt, Emma;
Murch, Ashleigh

Publication type:

Article

Limb defects and chorionic villus sampling: Are they linked?

Published in:

Patient Care (Print), 1996, v. 30, n. 13, p. 222

By:

Pinkowish, Mary Desmond

Publication type:

Article

Confirmation and characterization of interspecific hybrids of Passiflora L. (Passifloraceae) for ornamental use.

Published in:

Euphytica, 2012, v. 184, n. 3, p. 389, doi. 10.1007/s10681-011-0607-7

By:

Santos, Eileen;
Souza, Margarete;
Abreu, Priscilla;
da Conceição, Leo;
Araújo, Ioná;
Viana, Alexandre;
Almeida, Alex-Alan;
Freitas, Jôsie

Publication type:

Article

Surgical treatment of interhemispheric arachnoid cysts.

Published in:

Child's Nervous System, 2024, v. 40, n. 4, p. 1169, doi. 10.1007/s00381-023-06243-1

By:

Kim, Tae-Kyun;
Kim, Joo Whan;
Kim, Seung-Ki;
Lee, Ji Yeoun;
Kim, Kyung Hyun;
Phi, Ji Hoon

Publication type:

Article

Ante-natal counseling in phacomatoses.

Published in:

Child's Nervous System, 2020, v. 36, n. 10, p. 2269, doi. 10.1007/s00381-020-04776-3

By:

Brabbing-Goldstein, Dana;
Ben-Shachar, Shay

Publication type:

Article

Genetic analysis prior to selective fetal reduction in multiple pregnancy: technical aspects and clinical outcome.

Published in:

1995

By:

Brambati, B;
Tului, L;
Baldi, M;
Guercilena, S

Publication type:

journal article

Preimplantation diagnosis or chorionic villus biopsy? Women's attitudes and preferences.

Published in:

1993

By:

Miedzybrodzka, Z;
Templeton, A;
Dean, J;
Haites, N;
Mollison, J;
Smith, N

Publication type:

journal article

Prenatal diagnosis of Sex determining region Y-box transcription factor 2 anophthalmia syndrome caused by germline mosaicism using next-generation sequencing: A case report.

Published in:

International Journal of Reproductive Biomedicine, 2023, v. 21, n. 8, p. 667, doi. 10.18502/ijrm.v21i8.14022

By:

Nikuei, Pooneh;
Khashavy, Zahra;
Fard, Mohammad Ali Farazi;
Tabasi, Shahrzad;
Zeidi, Ari;
Pourkashani, Parnian;
Tabatabaei, Zahra;
Eftekhar, Ebrahim;
Saberi, Mozhgan;
Mahjoubi, Frouzandeh

Publication type:

Article

Prenatal diagnosis of citrullinemia type 1; seven families with c.1168G>A mutation of Argininosuccinate synthetase 1 gene in Southwest Iran: A case series.

Published in:

International Journal of Reproductive Biomedicine, 2022, v. 20, n. 12, p. 1047, doi. 10.18502/ijrm.v20i12.12567

By:

Hassanlou, Maryam;
Abiri, Maryam;
Zeinali, Sirous

Publication type:

Article

Is cervical swab an efficient method for developing a new noninvasive prenatal diagnostic test for numerical and structural chromosome anomalies?

Published in:

Turkish Journal of Medical Sciences, 2021, v. 51, n. 3, p. 1043, doi. 10.3906/sag-2009-347

By:

YURTCU, Erkan;
KARÇAALTINCABA, Deniz;
KAZAN, Hasan Hüseyin;
ÖZDEMİR, Halis;
YİRMİBEŞ KARAOĞUZ, Meral;
ÇALIŞ, Pınar;
KAYHAN, Gülsüm;
GÜNTEKİN ERGÜN, Sezen;
PERÇİN, Ferda;
BAYRAM, Merih;
İLHAN, Mustafa Necmi;
BİLGİLİ, Gamze;
KAYMAK, Tuğrul;
ERGÜN, Mehmet Ali

Publication type:

Article

Evaluation of the results of patients who applied to the Çukurova University, Medical Genetics Department for prenatal diagnosis and determination of genetic counseling principles.

Published in:

Turkish Journal of Medical Sciences, 2021, v. 51, n. 2, p. 657, doi. 10.3906/sag-2004-298

By:

TUĞ BOZDOĞAN, Sevcan;
BÜYUKKURT, Selim;
ÖZER, Sinem;
BİŞGİN, Atıl

Publication type:

Article

Prenatal diagnosis of phenylketonuria: a tertiary center experience.

Published in:

Obstetrică şi Ginecologie, 2024, v. 72, n. 3, p. 132

By:

Beksac, Mehmet Sinan;
Yılmaz, Engin;
Coşkun, Turgay;
Ozguc, Meral;
Cakar, Ayse Nur;
Gurbuz, Berrak Bilginer;
Aydin, Emine;
Buyukeren, Melek;
Orgul, Gokcen;
Ozalp, Imran

Publication type:

Article

Prenatal Diagnosis: A critical review of methods.

Published in:

South Asian Journal of Experimental Biology, 2020, v. 10, n. 6, p. 491, doi. 10.38150/sajeb.10(6).p491-510

By:

Bhagat, Neeta;
Singh, Sohini;
Andress, Allena;
Allen, Tanu

Publication type:

Article

An Update on Current Prenatal Testing Options: First Trimester and Noninvasive Prenatal Testing.

Published in:

2015

By:

Latendresse, Gwen;
Deneris, Angela

Publication type:

Journal Article

B - 02 The Impact of Cardiovascular Surgeries on Attention and Executive Functioning Outcomes in Children with Congenital Heart Defects with and without Attention-Deficit/Hyperactivity Disorder (ADHD) Diagnoses.

Published in:

2023

By:

Bean, Akanksha M;
Robinson, Mary L;
Krapf, Erica M;
Hassara, Kathleen E;
Schneider, Bruna M

Publication type:

Abstract

Prenatal diagnosis and preimplantation genetics testing of 3M syndrome in a Chinese family with novel biallelic variants of CUL7.

Published in:

2024

By:

Wang, Xueqian;
He, Yaqiong;
Wang, Xiaorong;
Kong, Xiangtian;
Lin, Yunying;
Yao, Yejie;
Huang, Yi

Publication type:

Case Study

Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1621

By:

Gabriel, Marie Cosette;
Rice, Stephanie M.;
Sloan, Jennifer L.;
Mossayebi, Matthew H.;
Venditti, Charles P.;
Al‐Kouatly, Huda B.

Publication type:

Article

Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1446

By:

Wang, Yan;
Zhang, Min;
Chen, Lingji;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Monochorionic diamniotic twins of discordant external genitalia with 45,X/46,XY mosaicism.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1382

By:

Takahashi, Ken;
Sato, Taisuke;
Nishiyama, Miyuki;
Sasaki, Aiko;
Taniguchi, Kosuke;
Migita, Ohsuke;
Wada, Seiji;
Hata, Kenichiro;
Sago, Haruhiko

Publication type:

Article

A glimpse of women's health in China.

Published in:

New Zealand Medical Student Journal, 2018, n. 26, p. 41

By:

Wang, Danni

Publication type:

Article

Population-based trends in invasive prenatal diagnosis for ultrasound-based indications: two decades of change from 1994 to 2016.

Published in:

2019

By:

Lostchuck, E.;
Poulton, A.;
Halliday, J.;
Hui, L.

Publication type:

journal article

Procedural and obstetric outcomes after embryo reduction vs fetal reduction in multifetal pregnancy.

Published in:

2019

By:

Kim, M. S.;
Ahn, E.;
Cho, H. Y.;
Baek, M. J.;
Moon, M. J.;
Choi, D. H.;
Kwon, H.;
Shin, J. E.;
Kim, Mi Sun;
Ahn, Eunhee;
Cho, Hee Young;
Baek, Min Jung;
Moon, Myoung Jin;
Choi, Dong Hee;
Kwon, Hwang;
Shin, Ji Eun

Publication type:

journal article

EP11.12: Antenatal diagnosis of Miller‐McKusick‐Malvaux (3‐M) syndrome: a case report.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 246, doi. 10.1002/uog.19972

By:

Yulia, A.;
Chelemen, O.;
Pandya, P.

Publication type:

Article

EP02.10: Placental mosaicism and early oligohydramnios: a case report.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 199, doi. 10.1002/uog.19804

By:

Sepp, K.;
Ustav, E.

Publication type:

Article

P20.10: Risk of fetal loss in pregnancies undergoing mid‐trimester amniocentesis after inconclusive chorionic villus sampling.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 194, doi. 10.1002/uog.19786

By:

Salsi, G.;
Grati, F.;
Bellussi, F.;
Pompilii, E.;
Maggi, F.;
Simoni, G.;
D'Ambrosi, F.;
Orsi, M.;
Fanelli, T.;
Rembouskos, G.;
Volpe, P.;
Gentile, M.;
Persico, N.;
Pilu, G.

Publication type:

Article

P20.08: Correlation of fetal ultrasonographic findings in prenatally diagnosed de novo balanced translocations.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 192, doi. 10.1002/uog.19784

By:

Seong, E.;
Boo, H.;
Kwak, D.;
Kim, M.;
Chung, J.;
Ryu, H.;
Han, Y.

Publication type:

Article

P20.06: The experience with whole‐genome array as a first‐line cytogenetic test in invasive prenatal diagnosis.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 192, doi. 10.1002/uog.19782

By:

Hynek, M.;
Trkova, M.;
Becvarova, V.;
Brezinova, S.;
Smetanova, D.;
Pekova, H.;
Mansfeldova, R.;
Koudova, M.;
Horacek, J.

Publication type:

Article

P19.02: Procedural and obstetrical outcomes of amniocentesis or chorionic villus sampling in dichorionic twin pregnancies.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 187, doi. 10.1002/uog.19768

By:

Kim, M.;
Moon, M.;
Jung, S.;
Chang, S.;
Kang, S.;
Ahn, E.

Publication type:

Article

OP02.02: Placental mesenchymal dysplasia with hepatic mesenchymal hamartoma: a case report.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 69, doi. 10.1002/uog.19402

By:

Boo, H.;
Chung, J.;
Han, Y.;
Kim, M.;
Lee, Y.

Publication type:

Article

OP01.01: The impact of introducing non‐invasive prenatal screening (NIPS) into routine prenatal care on timing of first ultrasound and on diagnostic testing.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 66, doi. 10.1002/uog.19391

By:

Doulaveris, G.;
Goldwaser, T.;
Gebb, J.;
Bernstein, P.;
Klugman, S.;
Dar, P.

Publication type:

Article

OC14.01: Do chorionic villus sampling (CVS) or amniocentesis (AC) induce rhesus immunisation? An evaluation of a cohort with no prophylaxis after CVS or AC.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 32, doi. 10.1002/uog.19296

By:

Kristensen, S.S.;
Nørgaard, L.N.;
Tabor, A.;
Dziegiel, M.;
Sundberg, K.;
Ekelund, C.K.

Publication type:

Article

OC02.01: The evolution of ultrasound‐indicated prenatal diagnosis over the past two decades: a state‐wide retrospective cohort study from 1994–2016.

Published in:

Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 3, doi. 10.1002/uog.19212

By:

Lostchuck, E.;
Poulton, A.;
Halliday, J.;
Hui, L.

Publication type:

Article

Chromosomal microarray as primary diagnostic genomic tool for pregnancies at increased risk within a population-based combined first-trimester screening program.

Published in:

2018

By:

Vogel, I.;
Vestergaard, E. M.;
Christensen, R.;
Petersen, O. B.;
Lou, S.;
Hyett, J.

Publication type:

journal article

OP23.02: Percutaneous transvesical chorionic villus sampling: an alternative method for difficult procedures.

Published in:

Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 122, doi. 10.1002/uog.17909

By:

Cavoretto, P.I.;
Giorgione, V.;
Inversetti, A.;
Candiani, M.

Publication type:

Article

EP06.15: Early and late chorionic villus sampling in Zagreb: experience with 13,300 cases.

Published in:

Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 287, doi. 10.1002/uog.18419

By:

Podobnik, M.;
Podobnik Brlecic, P.;
Gebauer Vuković, B.;
Brlečić, I.

Publication type:

Article

Total pregnancy loss after chorionic villus sampling and amniocentesis: a cohort study.

Published in:

2017

By:

Bakker, M.;
Birnie, E.;
Robles de Medina, P.;
Sollie, K. M.;
Pajkrt, E.;
Bilardo, C. M.

Publication type:

journal article

OP21.09: Risk factors for miscarriage after chorionic villus sampling.

Published in:

Ultrasound in Obstetrics & Gynecology, 2016, v. 48, p. 121, doi. 10.1002/uog.16364

By:

Hynek, M.;
Smetanova, D.;
Stejskal, D.

Publication type:

Article

EP09.05: Early amniocentesis: CVS alternative?

Published in:

2016

By:

Al Ibrahim, A.A.;
Zidan, M.;
Al-Obaidly, S.;
Khenyab, N.

Publication type:

journal article

ISUOG Practice Guidelines: invasive procedures for prenatal diagnosis.

Published in:

2016

By:

Ghi, T.;
Sotiriadis, A.;
Calda, P.;
Da Silva Costa, F.;
Raine‐Fenning, N.;
Alfirevic, Z.;
McGillivray, G.

Publication type:

journal article

Confined placental mosaicism of double trisomies 9 and 21: discrepancy between non-invasive prenatal testing, chorionic villus sampling and postnatal confirmation.

Published in:

2016

By:

Cheng, H.‐H.;
Ma, G.‐C.;
Tsai, C.‐C.;
Wu, W.‐J.;
Lan, K.‐C.;
Hsu, T.‐Y.;
Yang, C.‐W.;
Chen, M.

Publication type:

Case Study

IONA test for first-trimester detection of trisomies 21, 18 and 13.

Published in:

2016

By:

Poon, L. C.;
Dumidrascu‐Diris, D.;
Francisco, C.;
Fantasia, I.;
Nicolaides, K. H.;
Dumidrascu-Diris, D

Publication type:

journal article

Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies.

Published in:

2016

By:

Li, R.;
Wan, J.;
Zhang, Y.;
Fu, F.;
Ou, Y.;
Jing, X.;
Li, J.;
Li, D.;
Liao, C.

Publication type:

journal article

How to safeguard competency and training in invasive prenatal diagnosis: 'the elephant in the room'.

Published in:

2016

By:

Hui, L.;
Tabor, A.;
Walker, S. P.;
Kilby, M. D.

Publication type:

Editorial

Risk of fetal loss associated with invasive testing following combined first-trimester screening for Down syndrome: a national cohort of 147,987 singleton pregnancies.

Published in:

2016

By:

Wulff, C. B.;
Gerds, T. A.;
Rode, L.;
Ekelund, C. K.;
Petersen, O. B.;
Tabor, A.;
Zingenberg, H.;
Jørgensen, F. S.;
Sundberg, K.;
Shalmi, A. ‐C.;
Näslund Thagaard, I.;
Skibsted, L.;
Fabricius, M.;
Sperling, L.;
Mogensen, H.;
Ibsen, M.;
Brendstrup, L.;
Jensen, H. S.;
Kamper, C. H.;
Vase, L.

Publication type:

journal article

Re: Risk of fetal loss associated with invasive testing following combined first-trimester screening for Down syndrome: a national cohort of 147 987 singleton pregnancies. C. B. Wulff, T. A. Gerds, L. Rode, C. K. Ekelund, O. B. Petersen, A. Tabor and the Danish Fetal Medicine Study Group. Ultrasound Obstet Gynecol 2016; 47: 38-44.

Published in:

2016

By:

Akolekar, R.

Publication type:

journal article

Re: Risk of miscarriage following amniocentesis and chorionic villus sampling.

Published in:

Ultrasound in Obstetrics & Gynecology, 2015, v. 45, n. 6, p. 755, doi. 10.1002/uog.14850

By:

Ghidini, A.

Publication type:

Article