Works matching DE "PRENATAL diagnosis"

Results: 5000

Fathers of children born with cleft lip and palate: Impact of the timing of diagnosis.

Published in:

2016

By:

Zeytinoğlu, Senem;
Davey, Maureen P.;
Crerand, Canice;
Fisher, Kathleen

Publication type:

Journal Article

Enhancing maternal depression recognition in health care settings: A review of strategies to improve detection, reduce barriers, and reach mothers in need.

Published in:

2012

By:

Freed, Rachel D.;
Chan, Priscilla T.;
Boger, Kathryn Dingman;
Tompson, Martha C.

Publication type:

Journal Article

Discrepant feeling rules and unscripted emotion work: Women coping with termination for fetal anomaly.

Published in:

2009

By:

McCoyd, Judith L. M.

Publication type:

Journal Article

Understanding pregnant women's decision making concerning prenatal screening.

Published in:

2008

By:

van den Berg, Matthijs;
Timmermans, Danielle R. M.;
Knol, Dirk L.;
van Eijk, Jacques Th. M.;
de Smit, Denhard J.;
van Vugt, John M. G.;
van der Wal, Gerrit

Publication type:

Journal Article

Prenatal development of intrafetal and maternal-fetal synchrony.

Published in:

2006

By:

DiPietro, Janet A.;
Caulfield, Laura E.;
Irizarry, Rafael A.;
Chen, Ping;
Merialdi, Mario;
Zavaleta, Nelly

Publication type:

Journal Article

Genetic testing: Psychological aspects and implications.

Published in:

2002, isbn. 1-55798-933-8

By:

Lerman, Caryn;
Croyle, Robert T.;
Tercyak, Kenneth P.;
Hamann, Heidi

Publication type:

Journal Article

Reactions to prenatal diagnosis: An analysis of 87 interviews.

Published in:

1980

By:

Silvestre, Danielle;
Fresco, Nadine

Publication type:

Journal Article

The epidemiology and prevention of mental retardation.

Published in:

1987

By:

Scott, Keith G.;
Carran, Deborah T.

Publication type:

Journal Article

A study in the cause and prevention of functional mental disease.

Published in:

1938

By:

Dershimer, Frederick W.

Publication type:

Journal Article

奶牛早期妊娠诊断技术的应用进展.

Published in:

China Herbivore Science, 2025, v. 45, n. 3, p. 80, doi. 10.3969/j.issn.2095-3887.2024.00.144

By:

郝海生

Publication type:

Article

Utility of Biometric Measurements from Fetal Magnetic Resonance Imaging for Improved Antenatal Diagnosis of Dandy–Walker Spectrum Posterior Fossa Lesions.

Published in:

Diagnostics (2075-4418), 2025, v. 15, n. 10, p. 1295, doi. 10.3390/diagnostics15101295

By:

Bowker, Rakhee M.;
Marathu, Kranthi K.;
Pharel, Marissa;
Adepoju, Jubril O.;
Vahedifard, Farzan;
Adler, Seth;
Kocak, Mehmet;
Liu, Xuchu;
Byrd, Sharon E.

Publication type:

Article

Application of Whole-Exome Sequencing (WES) for Prenatal Determination of Causes of Fetal Abnormalities.

Published in:

Genes, 2025, v. 16, n. 5, p. 547, doi. 10.3390/genes16050547

By:

Guseva, Margarita;
Shirokova, Natalya;
Kapitonova, Olga;
Gnetetskaya, Valentina;
Blagodatskikh, Konstantin;
Tarasova, Julia;
Kaimonov, Vladimir;
Korbut, Alina;
Musatova, Elizaveta

Publication type:

Article

Molecular genetics of beta-thalassaemia syndrome in Pakistan.

Published in:

Eastern Mediterranean Health Journal, 2010, v. 16, n. 9, p. 972, doi. 10.26719/2010.16.9.972

By:

Usman, M.;
Moinuddin, M.;
Ghani, R.

Publication type:

Article

Unilateral, frontal polymicrogyria and supratentorial white matter microcysts in fetus with Joubert syndrome and related disorders: Prenatal diagnosis with magnetic resonance imaging.

Published in:

Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2020, v. 77, n. 10, p. 1093, doi. 10.2298/VSP180906173K

By:

Koprivšek, Katarina;
Bjelan, Mladen;
Lučić, Miloš;
Šveljo, Olivera;
Kostić, Dejan;
Kozić, Duško

Publication type:

Article

Prenatal ultrasonographic manifestations of partial trisomy 12q(12q24.2→qter) and partial monosomy 2q (2q37.3→qter).

Published in:

Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2020, v. 77, n. 7, p. 754, doi. 10.2298/VSP170316136J

By:

Joksić, Ivana;
Liehr, Thomas;
Toljić, Mina;
Karadzov-Orlić, Nataša;
Milovanović, Zagorka;
Miković, Željko;
Egić, Amira

Publication type:

Article

The role of information provision in economic evaluations of non-invasive prenatal testing: a systematic review.

Published in:

2019

By:

John, Nikita M.;
Wright, Stuart J.;
Gavan, Sean P.;
Vass, Caroline M.

Publication type:

journal article

Cost-effectiveness of cell-free DNA in maternal blood testing for prenatal detection of trisomy 21, 18 and 13: a systematic review.

Published in:

2018

By:

García-Pérez, Lidia;
Linertová, Renata;
Álvarez-de-la-Rosa, Margarita;
Bayón, Juan Carlos;
Imaz-Iglesia, Iñaki;
Ferrer-Rodríguez, Jorge;
Serrano-Aguilar, Pedro

Publication type:

journal article

Cost-effectiveness of rapid syphilis screening in prenatal HIV testing programs in Haiti.

Published in:

2007

By:

Schackman, Bruce R.;
Neukermans, Christopher P.;
Fontain, Sandy N. Nerette;
Nolte, Claudine;
Joseph, Patrice;
Pape, Jean W.;
Fitzgerald, Daniel W.

Publication type:

journal article

High Risk of Unexpected Late Fetal Death in Monochorionic Twins Despite Intensive Ultrasound Surveillance: A Cohort Study.

Published in:

PLoS Medicine, 2005, v. 2, n. 6, p. 0521, doi. 10.1371/journal.pmed.0020172

By:

Barigye, Olivia;
Pasquini, Lucia;
Galea, Paula;
Chambers, Helen;
Chappell, Lucy;
Fisk, Nicholas M.

Publication type:

Article

Attitudes of pregnant women and mothers of children with orofacial clefts toward prenatal diagnosis of nonsyndromic orofacial clefts in a semiurban set-up in India.

Published in:

Indian Journal of Plastic Surgery, 2011, v. 44, n. 3, p. 489, doi. 10.4103/0970-0358.90833

By:

Kadagad, Poornima;
Pinto, Pascal;
Powar, Rajesh

Publication type:

Article

Elective Uniportal Video-Assisted Thoracoscopic Lobectomy for Congenital Cystic Lung Disease in a 2-Year-Old Child Using One-Lung Ventilation.

Published in:

Indian Journal of Surgery, 2023, v. 85, p. 552, doi. 10.1007/s12262-022-03397-1

By:

Shiiya, Haruhiko;
Ujiie, Hideki;
Kato, Tatsuya;
Honda, Shohei;
Wakasa, Satoru;
Kaga, Kichizo

Publication type:

Article

Congenital Hypothyroidism with Neuronal Migration Anomaly.

Published in:

Neurology India, 2024, v. 72, n. 2, p. 462, doi. 10.4103/neurol-india.Neurol-India-D-24-00195

By:

Maivizhi, Shruthi M.;
Sahoo, Biswajit;
Nayak, Manoj Kumar

Publication type:

Article

Prenatal Ventriculomegaly - Diagnosis, Prognostication and Management.

Published in:

2021

By:

Krishnan, Vivek;
Sharma, Akshatha;
Ramamurthy, Rachita;
Elayedatt, Rinshi;
Ramamurthy, B;
Ramamurthy, B S

Publication type:

journal article

Clinical and Mutation Spectra of Cockayne Syndrome in India.

Published in:

2021

By:

Narayanan, Dhanya;
Tuteja, Moni;
McIntyre, Adam;
Hegele, Robert;
Calmels, Nadege;
Obringer, Cathy;
Laugel, Vincent;
Mandal, Kausik;
Phadke, Shubha;
Narayanan, Dhanya L;
McIntyre, Adam D;
Hegele, Robert A;
Phadke, Shubha R

Publication type:

journal article

Technological experiences and end-users' identification work – investigating expectant mothers' prenatal ultrasound experiences and their reconfigurations.

Published in:

Social Identities, 2023, v. 29, n. 2, p. 130, doi. 10.1080/13504630.2023.2208037

By:

Yeh, Hsin-Yi

Publication type:

Article

Prenatal diagnosis following preimplantation genetic testing for monogenic conditions: a single centre record linkage study.

Published in:

Journal of Assisted Reproduction & Genetics, 2025, v. 42, n. 1, p. 275, doi. 10.1007/s10815-024-03346-9

By:

Poulton, Alice;
Menezes, Melody;
Hardy, Tristan;
Lewis, Sharon;
Hui, Lisa

Publication type:

Article

Extended application of PGT-M strategies for small pathogenic CNVs.

Published in:

Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 3, p. 739, doi. 10.1007/s10815-024-03028-6

By:

Hu, Xiao;
Wang, Weili;
Luo, Keli;
Dai, Jing;
Zhang, Yi;
Wan, Zhenxing;
He, Wenbin;
Zhang, Shuoping;
Yang, Lanlin;
Tan, Qin;
Li, Wen;
Zhang, Qianjun;
Gong, Fei;
Lu, Guangxiu;
Tan, Yue-Qiu;
Lin, Ge;
Du, Juan

Publication type:

Article

Exploring attitudes and experiences with reproductive genetic carrier screening among couples seeking medically assisted reproduction: a longitudinal survey study.

Published in:

Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 2, p. 451, doi. 10.1007/s10815-023-03010-8

By:

Van Steijvoort, Eva;
Cassou, Mathilde;
De Schutter, Camille;
Dimitriadou, Eftychia;
Peeters, Hilde;
Peeraer, Karen;
Matthijs, Gert;
Borry, Pascal

Publication type:

Article

Prenatal diagnosis of a case with complete and uniform tetrasomy 12p by the utility of noninvasive prenatal testing.

Published in:

Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 9, p. 2233, doi. 10.1007/s10815-023-02896-8

By:

Zhang, Fang;
Yin, Ting;
Tang, Xinxin;
Ma, Shanshan;
Meng, Qian;
Song, Jiedong;
Wang, Yongan;
Men, Shuai;
Wang, Leilei

Publication type:

Article

Performance of noninvasive prenatal testing for twin pregnancies in South China.

Published in:

Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 9, p. 2219, doi. 10.1007/s10815-023-02881-1

By:

Wang, Dongmei;
Peng, Haishan;
Wang, Yixia;
Hou, Yaping;
Guo, Fangfang;
Zhu, Juan;
Hu, Tingting;
Yang, Jiexia

Publication type:

Article

Knowledge, acceptability and personal attitude toward pre-implantation 1 genetic testing (PGT) and pre-natal diagnosis (PND) for females carrying BRCA pathogenic variant according to fertility preservation experience.

Published in:

Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 6, p. 1381, doi. 10.1007/s10815-023-02798-9

By:

Dervin, Traicie;
Ranisavjevic, Noémie;
Laot, Lucie;
Mayeur, Anne;
Duperier, Constance;
Steffann, Julie;
Borghese, Roxana;
Stoppa-Lyonnet, Dominique;
Frydman, Nelly;
Benachi, Alexandra;
Sonigo, Charlotte;
Grynberg, Michael

Publication type:

Article

Cost-effectiveness of IVF with PGT-M/A to prevent transmission of spinal muscular atrophy in offspring of carrier couples.

Published in:

Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 4, p. 793, doi. 10.1007/s10815-023-02738-7

By:

Khorshid, Arian;
Boyd, Alleigh L. H.;
Behr, Barry;
Zhao, Qianying;
Alvero, Ruben;
Bavan, Brindha

Publication type:

Article

Combined fetal fraction to analyze the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18, and 21.

Published in:

Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 4, p. 803, doi. 10.1007/s10815-022-02694-8

By:

Yang, Jiexia;
Wu, Jing;
Wang, Dongmei;
Hou, Yaping;
Guo, Fangfang;
Zhang, Qi;
Peng, Haishan;
Wang, Yixia;
Yin, Aihua

Publication type:

Article

BRCA1/2 pathogenetic variant carriers and reproductive decisions: Gender differences and factors associated with the choice of preimplantation genetic diagnosis (PGD) and prenatal diagnosis (PND).

Published in:

Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 7, p. 1433, doi. 10.1007/s10815-022-02523-y

By:

Lombardi, Lucia;
Trumello, Carmen;
Stuppia, Liborio;
Antonucci, Ivana;
Brandão, Tânia;
Babore, Alessandra

Publication type:

Article

Genetic counseling decisions in gestational carrier pregnancies.

Published in:

Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 6, p. 1249, doi. 10.1007/s10815-022-02483-3

By:

Rasouli, Melody A.;
Roberts, Hailey E.;
Jackson, David N.

Publication type:

Article

Cell-based non-invasive prenatal testing for monogenic disorders: confirmation of unaffected fetuses following preimplantation genetic testing.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 8, p. 1959, doi. 10.1007/s10815-021-02104-5

By:

Toft, Christian Liebst Frisk;
Ingerslev, Hans Jakob;
Kesmodel, Ulrik Schiøler;
Hatt, Lotte;
Singh, Ripudaman;
Ravn, Katarina;
Nicolaisen, Bolette Hestbek;
Christensen, Inga Baasch;
Kølvraa, Mathias;
Jeppesen, Line Dahl;
Schelde, Palle;
Vogel, Ida;
Uldbjerg, Niels;
Farlie, Richard;
Sommer, Steffen;
Østergård, Marianne Louise Vang;
Jensen, Ann Nygaard;
Mogensen, Helle;
Kjartansdóttir, Kristín Rós;
Degn, Birte

Publication type:

Article

Noninvasive prenatal detection of fetal sex chromosome abnormalities using the semiconductor sequencing platform (SSP) in Southern China.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 3, p. 727, doi. 10.1007/s10815-020-02056-2

By:

Yang, Jiexia;
Hou, Yaping;
Guo, Fangfang;
Peng, Haishan;
Wang, Dongmei;
Li, Yi;
OY, Haoxin;
Wang, Yixia;
Lu, Jian;
Yin, Aihua

Publication type:

Article

Next-generation sequencing: a follow-up of 36,913 singleton pregnancies with noninvasive prenatal testing in central China.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 12, p. 3143, doi. 10.1007/s10815-020-01977-2

By:

Lu, Wan;
Huang, Ting;
Wang, Xin-Rong;
Zhou, Ji-Hui;
Yuan, Hui-Zhen;
Yang, Yan;
Huang, Ting-Ting;
Liu, Dan-Ping;
Liu, Yan-Qiu

Publication type:

Article

In-house genetic counseling increases the detection of abnormal karyotypes—a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 8, p. 1999, doi. 10.1007/s10815-020-01812-8

By:

Bijok, Julia;
Kucińska–Chahwan, Anna;
Massalska, Diana;
Ilnicka, Alicja;
Panek, Grzegorz;
Roszkowski, Tomasz

Publication type:

Article

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.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 8, p. 2019, doi. 10.1007/s10815-020-01825-3

By:

Okmen, Firat;
Ekici, Huseyin;
Hortu, Ismet;
Imamoglu, Metehan;
Arican, Duygu;
Akın, Haluk;
Sagol, Sermet

Publication type:

Article

A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 3, p. 573, doi. 10.1007/s10815-020-01690-0

By:

Bellil, Hela;
Herve, Bérenice;
Herzog, Elodie;
Ayoubi, Jean-Marc;
Vialard, François;
Poulain, Marine

Publication type:

Article

The clinical application of preimplantation genetic diagnosis for X-linked retinitis pigmentosa.

Published in:

Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 5, p. 989, doi. 10.1007/s10815-019-01434-9

By:

Huang, Xinghua;
Liu, Yun;
Yu, Xiurong;
Huang, Qiuxiang;
Lin, Chunli;
Zeng, Jian;
Lan, Fenghua;
Wang, Zhihong

Publication type:

Article

Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome.

Published in:

Journal of Assisted Reproduction & Genetics, 2018, v. 35, n. 6, p. 985, doi. 10.1007/s10815-018-1228-z

By:

Johnson, John P.;
Beischel, Linda;
Schwanke, Corbin;
Styren, Katie;
Crunk, Amy;
Schoof, Jonathan;
Elias, Abdallah F.

Publication type:

Article

Detection of a case of Angelman syndrome caused by an imprinting error in 949 pregnancies analyzed for AS following IVF.

Published in:

2018

By:

Johnson, John P.;
Schoof, Jonathon;
Beischel, Linda;
Schwancke, Corbin;
Goldberg, James;
Black, Lauri;
Ross, Lori;
Bhatt, Suchina

Publication type:

Case Study

Mosaic embryo transfer after oocyte in vitro maturation in combination with non-invasive prenatal testing (NIPT)-first report of a euploid live birth.

Published in:

Journal of Assisted Reproduction & Genetics, 2017, v. 34, n. 9, p. 1199, doi. 10.1007/s10815-017-0974-7

By:

Inoue, Naomi;
Lopez, Rosmary;
Delgado, Andrea;
Nuñez, Denisse;
Portella, Jimmy;
Noriega-Hoces, Luis;
Guzmán, Luis

Publication type:

Article

Prenatal screening for chromosomal abnormalities in IVF patients that opted for preimplantation genetic screening/diagnosis (PGS/D): a need for revised algorithms in the era of personalized medicine.

Published in:

Journal of Assisted Reproduction & Genetics, 2017, v. 34, n. 6, p. 723, doi. 10.1007/s10815-017-0907-5

By:

Takyi, Afua;
Santolaya-Forgas, Joaquin

Publication type:

Article

Comparison of intrafollicular sperm injection and intrauterine insemination in the treatment of subfertility.

Published in:

Journal of Assisted Reproduction & Genetics, 2012, v. 29, n. 10, p. 1103, doi. 10.1007/s10815-012-9836-5

By:

Lucchini, Caterina;
Volpe, Emanuele;
Tocci, Angelo

Publication type:

Article

Prenatal diagnosis of Comel-Netherton syndrome with PGD, case report and review article.

Published in:

2011

By:

Bingol, Banu;
Tasdemir, Seval;
Gunenc, Ziya;
Abike, Faruk;
Esenkaya, Semra;
Tavukcuoglu, Safak;
Berkil, Hakan

Publication type:

Report

Non-invasive prenatal detection of achondroplasia using circulating fetal DNA in maternal plasma.

Published in:

Journal of Assisted Reproduction & Genetics, 2011, v. 28, n. 2, p. 167, doi. 10.1007/s10815-010-9489-1

By:

Lim, Ji;
Kim, Mee;
Kim, Shin;
Kim, Hye;
Song, Mee;
Kim, Min;
Park, So;
Yang, Jae;
Ryu, Hyun

Publication type:

Article

Maternal antimullerian hormone levels do not predict fetal aneuploidy.

Published in:

Journal of Assisted Reproduction & Genetics, 2010, v. 27, n. 7, p. 409, doi. 10.1007/s10815-010-9433-4

By:

Plante, Beth J.;
Beamon, Carmen;
Schmitt, Colleen L.;
Moldenhauer, Julie S.;
Steiner, Anne Z.

Publication type:

Article