Works matching IS 01973851 AND DT 2021 AND VI 41 AND IP 6

Results: 36

The prognosis of common arterial trunk from a fetal perspective: A prenatal cohort study and systematic literature review.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 754, doi. 10.1002/pd.5907

By:

van Nisselrooij, Amber E. L.;
Herling, Lotta;
Clur, Sally‐Ann;
Linskens, Ingeborg H.;
Pajkrt, Eva;
Rammeloo, Lukas A.;
ten Harkel, Arend D. J.;
Hazekamp, Mark G.;
Blom, Nico A.;
Haak, Monique C.

Publication type:

Article

Ultrasound diagnosis of oculo-auriculo-vertebral spectrum in a mid-trimester foetus.

Published in:

2021

By:

Song, Qing‐Yun;
Luo, Hong;
Song, Qing-Yun

Publication type:

Letter

The diagnostic efficacy of exome data analysis using fixed neurodevelopmental gene lists: Implications for prenatal setting.

Published in:

2021

By:

Sukenik‐Halevy, Rivka;
Ruhrman‐Shahar, Noa;
Orenstein, Naama;
Gonzaga‐Jauregui, Claudia;
Shuldiner, Alan R.;
Magal, Nurit;
Hagari, Ofir;
Azulay, Noy;
Lidzbarsky, Gabriel A.;
Bazak, Lily;
Basel‐Salmon, Lina;
Sukenik-Halevy, Rivka;
Ruhrman-Shahar, Noa;
Gonzaga-Jauregui, Claudia;
Lidzbarsky, Gabriel Arie;
Basel-Salmon, Lina

Publication type:

journal article

Health practitioners' perceptions of the barriers and enablers to the implementation of reproductive genetic carrier screening: A systematic review.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 708, doi. 10.1002/pd.5914

By:

Best, Stephanie;
Long, Janet;
Theodorou, Tahlia;
Hatem, Sarah;
Lake, Rebecca;
Archibald, Alison;
Freeman, Lucinda;
Braithwaite, Jeffrey

Publication type:

Article

Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionals.

Published in:

2021

By:

Lewis, Celine;
Hammond, Jennifer;
Klapwijk, Jasmijn E.;
Harding, Eleanor;
Lou, Stina;
Vogel, Ida;
Szepe, Emma J.;
Hui, Lisa;
Ingvoldstad‐Malmgren, Charlotta;
Soller, Maria J.;
Ormond, Kelly E.;
Choolani, Mahesh;
Hill, Melissa;
Riedijk, Sam;
Szepe, Emma Jane;
Ingvoldstad-Malmgren, Charlotta;
Soller, Maria Johansson

Publication type:

journal article

Fetoscopic urethral meatotomy in fetuses with lower urinary tract obstruction by congenital megalourethra.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 772, doi. 10.1002/pd.5946

By:

Cruz‐Martínez, Rogelio;
Martínez‐Rodríguez, Miguel;
Gámez‐Varela, Alma;
Luna‐García, Jonahtan;
López‐Briones, Hugo;
Chávez‐González, Erendira;
Villalobos‐Gómez, Rosa;
Juárez‐Martínez, Israel

Publication type:

Article

Prenatal chromosome microarray: 'The UK experience'. A survey of reporting practices in UK genetic services (2012–2019).

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 661, doi. 10.1002/pd.5944

By:

Patterson, Jenny;
Wellesley, Diana;
Morgan, Sian;
Cilliers, Deirdre;
Allen, Stephanie;
Gardiner, Carol A

Publication type:

Article

Prenatal diagnosis and postnatal management of congenital mesoblastic nephroma: Experience at a single center in China.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 766, doi. 10.1002/pd.5942

By:

Chen, Yan‐Xiong;
Huang, Chao;
He, Qiu‐Ming;
Wang, Zhe;
Huang, Li;
Wang, Hai‐Yu;
Mei, Shan‐Shan;
Chai, Cheng‐Wei;
Zhang, Guang‐Lan;
Zhong, Wei;
Li, Dong‐Zhi

Publication type:

Article

Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 652, doi. 10.1002/pd.5941

By:

Grati, Francesca Romana;
Malvestiti, Francesca;
Gallazzi, Gloria;
Saragozza, Silvia;
Grimi, Beatrice;
Agrati, Cristina;
Branca, Lara;
Palumbo, Federica;
Trotta, Anna;
Chinetti, Sara;
Simoni, Giuseppe;
Ferreira, Jose;
Benn, Peter

Publication type:

Article

Mosaicism for copy number variations in the placenta is even more difficult to interpret than mosaicism for whole chromosome aneuploidy.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 668, doi. 10.1002/pd.5938

By:

Lund, Ida C. Bay;
Becher, Naja;
Graakjaer, Jesper;
Lildballe, Dorte L.;
Uldbjerg, Niels;
Bogaard, Pauline;
Petersen, Astrid;
Vestergaard, Else M.;
Vogel, Ida

Publication type:

Article

Ultrasound diagnosis of oculo‐auriculo‐vertebral spectrum in a mid‐trimester foetus.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 791, doi. 10.1002/pd.5936

By:

Song, Qing‐Yun;
Luo, Hong

Publication type:

Article

Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross‐sectional study with healthcare professionals.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 720, doi. 10.1002/pd.5932

By:

Lewis, Celine;
Hammond, Jennifer;
Klapwijk, Jasmijn E.;
Harding, Eleanor;
Lou, Stina;
Vogel, Ida;
Szepe, Emma J.;
Hui, Lisa;
Ingvoldstad‐Malmgren, Charlotta;
Soller, Maria J.;
Ormond, Kelly E.;
Choolani, Mahesh;
Hill, Melissa;
Riedijk, Sam

Publication type:

Article

The diagnostic efficacy of exome data analysis using fixed neurodevelopmental gene lists: Implications for prenatal setting.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 701, doi. 10.1002/pd.5929

By:

Sukenik‐Halevy, Rivka;
Ruhrman‐Shahar, Noa;
Orenstein, Naama;
Gonzaga‐Jauregui, Claudia;
Shuldiner, Alan R.;
Magal, Nurit;
Hagari, Ofir;
Azulay, Noy;
Lidzbarsky, Gabriel A.;
Bazak, Lily;
Basel‐Salmon, Lina

Publication type:

Article

Health practitioners' perceptions of the barriers and enablers to the implementation of reproductive genetic carrier screening: A systematic review.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 708, doi. 10.1002/pd.5914

By:

Best, Stephanie;
Long, Janet;
Theodorou, Tahlia;
Hatem, Sarah;
Lake, Rebecca;
Archibald, Alison;
Freeman, Lucinda;
Braithwaite, Jeffrey

Publication type:

Article

Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 697, doi. 10.1002/pd.5911

By:

Yu, Florrie N. Y.;
Li, Elizabeth Y. Y.;
Kong, Meliza C. W.;
Ma, Teresa W. L.;
Chan, Kelvin Y. K.;
Man, Elim;
Chung, Brian H. Y.;
Kan, Anita S. Y.

Publication type:

Article

Prenatal diagnosis of diencephalic‐mesencephalic junction dysplasia: Fetal magnetic resonance imaging phenotypes, genetic diagnoses, and outcomes.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 778, doi. 10.1002/pd.5909

By:

Lawrence, Anne K.;
Whitehead, Matthew T.;
Kruszka, Paul;
Sanapo, Laura;
Yano, Sho;
Tanpaiboon, Pranoot;
Muenke, Maximilian;
Fraser, Jamie L.;
du Plessis, Adre J.

Publication type:

Article

Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 690, doi. 10.1002/pd.5908

By:

Junhui, Wan;
Ru, Li;
Qiuxia, Yu;
Dan, Wang;
Xiuhong, Sun;
Yongling, Zhang;
Xiangyi, Jing;
Fatao, Li;
Xuewei, Tang;
Guilan, Chen;
Fan, Jiang;
Fucheng, Li;
Fang, Fu;
Yan, Li;
Lina, Zhang;
Cuixing, Yi;
Jian, Li;
Dongzhi, Li;
Can, Liao

Publication type:

Article

Noninvasive screening for congenital heart defects using a serum metabolomics approach.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 743, doi. 10.1002/pd.5893

By:

Troisi, Jacopo;
Cavallo, Pierpaolo;
Richards, Sean;
Symes, Steven;
Colucci, Angelo;
Sarno, Laura;
Landolfi, Annamaria;
Scala, Giovanni;
Adair, David;
Ciccone, Carla;
Maruotti, Giuseppe M.;
Martinelli, Pasquale;
Guida, Maurizio

Publication type:

Article

Feasibility study of using unbalanced embryos as a reference to distinguish euploid carrier from noncarrier embryos by single nucleotide polymorphism array for reciprocal translocations.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 681, doi. 10.1002/pd.5897

By:

Li, Rong;
Wang, Jing;
Gu, Ailing;
Xu, Yan;
Guo, Jing;
Pan, Jiafu;
Zeng, Yanhong;
Ma, Yuanlin;
Zhou, Canquan;
Xu, Yanwen

Publication type:

Article

Artificial intelligence, fetal echocardiography, and congenital heart disease.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 733, doi. 10.1002/pd.5892

By:

Day, Thomas G.;
Kainz, Bernhard;
Hajnal, Jo;
Razavi, Reza;
Simpson, John M.

Publication type:

Article

Obituary: Bruno Brambati, MD (29 February 1940‐3 August 2020).

Published in:

2021

By:

Simoni, Prof Giuseppe

Publication type:

Obituary

Fetoscopic urethral meatotomy in fetuses with lower urinary tract obstruction by congenital megalourethra.

Published in:

2021

By:

Cruz‐Martínez, Rogelio;
Martínez‐Rodríguez, Miguel;
Gámez‐Varela, Alma;
Luna‐García, Jonahtan;
López‐Briones, Hugo;
Chávez‐González, Erendira;
Villalobos‐Gómez, Rosa;
Juárez‐Martínez, Israel;
Cruz-Martínez, R;
Martínez-Rodríguez, M;
Gámez-Varela, A;
Luna-García, J;
López-Briones, H;
Chávez-González, E;
Villalobos-Gómez, R;
Juárez-Martínez, I;
Cruz-Martínez, Rogelio;
Martínez-Rodríguez, Miguel;
Gámez-Varela, Alma;
Luna-García, Jonahtan

Publication type:

journal article

Issue Information.

Published in:: Prenatal Diagnosis, 2021, v. 41, n. 6, p. 649, doi. 10.1002/pd.5743
Publication type:: Article

Prenatal chromosome microarray: 'The UK experience'. A survey of reporting practices in UK genetic services (2012-2019).

Published in:

2021

By:

Patterson, Jenny;
Wellesley, Diana;
Morgan, Sian;
Cilliers, Deirdre;
Allen, Stephanie;
Gardiner, Carol A;
Fetal Genomics Steering Group;
UK Clinical Genetics Lead Clinician Group;
UK Heads of Genetics Laboratory Group

Publication type:

journal article

Prenatal diagnosis and postnatal management of congenital mesoblastic nephroma: Experience at a single center in China.

Published in:

2021

By:

Chen, Yan‐Xiong;
Huang, Chao;
He, Qiu‐Ming;
Wang, Zhe;
Huang, Li;
Wang, Hai‐Yu;
Mei, Shan‐Shan;
Chai, Cheng‐Wei;
Zhang, Guang‐Lan;
Zhong, Wei;
Li, Dong‐Zhi;
Chen, Yan-Xiong;
He, Qiu-Ming;
Wang, Hai-Yu;
Mei, Shan-Shan;
Chai, Cheng-Wei;
Zhang, Guang-Lan;
Li, Dong-Zhi

Publication type:

journal article

Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed.

Published in:

2021

By:

Grati, Francesca Romana;
Malvestiti, Francesca;
Gallazzi, Gloria;
Saragozza, Silvia;
Grimi, Beatrice;
Agrati, Cristina;
Branca, Lara;
Palumbo, Federica;
Trotta, Anna;
Chinetti, Sara;
Simoni, Giuseppe;
Ferreira, Jose;
Benn, Peter;
Grati, FrancescaRomana

Publication type:

journal article

Mosaicism for copy number variations in the placenta is even more difficult to interpret than mosaicism for whole chromosome aneuploidy.

Published in:

2021

By:

Lund, Ida C. Bay;
Becher, Naja;
Graakjaer, Jesper;
Lildballe, Dorte L.;
Uldbjerg, Niels;
Bogaard, Pauline;
Petersen, Astrid;
Vestergaard, Else M.;
Vogel, Ida;
Bay Lund, Ida Charlotte;
Vestergaard, Else Marie

Publication type:

journal article

Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases.

Published in:

2021

By:

Yu, Florrie N. Y.;
Li, Elizabeth Y. Y.;
Kong, Meliza C. W.;
Ma, Teresa W. L.;
Chan, Kelvin Y. K.;
Man, Elim;
Chung, Brian H. Y.;
Kan, Anita S. Y.

Publication type:

journal article

Prenatal diagnosis of diencephalic-mesencephalic junction dysplasia: Fetal magnetic resonance imaging phenotypes, genetic diagnoses, and outcomes.

Published in:

2021

By:

Lawrence, Anne K.;
Whitehead, Matthew T.;
Kruszka, Paul;
Sanapo, Laura;
Yano, Sho;
Tanpaiboon, Pranoot;
Muenke, Maximilian;
Fraser, Jamie L.;
du Plessis, Adre J.

Publication type:

journal article

Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 690, doi. 10.1002/pd.5908

By:

Junhui, Wan;
Ru, Li;
Qiuxia, Yu;
Dan, Wang;
Xiuhong, Sun;
Yongling, Zhang;
Xiangyi, Jing;
Fatao, Li;
Xuewei, Tang;
Guilan, Chen;
Fan, Jiang;
Fucheng, Li;
Fang, Fu;
Yan, Li;
Lina, Zhang;
Cuixing, Yi;
Jian, Li;
Dongzhi, Li;
Can, Liao

Publication type:

Article

The prognosis of common arterial trunk from a fetal perspective: A prenatal cohort study and systematic literature review.

Published in:

2021

By:

van Nisselrooij, Amber E. L.;
Herling, Lotta;
Clur, Sally‐Ann;
Linskens, Ingeborg H.;
Pajkrt, Eva;
Rammeloo, Lukas A.;
ten Harkel, Arend D. J.;
Hazekamp, Mark G.;
Blom, Nico A.;
Haak, Monique C.;
Clur, Sally-Ann

Publication type:

journal article

Feasibility study of using unbalanced embryos as a reference to distinguish euploid carrier from noncarrier embryos by single nucleotide polymorphism array for reciprocal translocations.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 681, doi. 10.1002/pd.5897

By:

Li, Rong;
Wang, Jing;
Gu, Ailing;
Xu, Yan;
Guo, Jing;
Pan, Jiafu;
Zeng, Yanhong;
Ma, Yuanlin;
Zhou, Canquan;
Xu, Yanwen

Publication type:

Article

Noninvasive screening for congenital heart defects using a serum metabolomics approach.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 743, doi. 10.1002/pd.5893

By:

Troisi, Jacopo;
Cavallo, Pierpaolo;
Richards, Sean;
Symes, Steven;
Colucci, Angelo;
Sarno, Laura;
Landolfi, Annamaria;
Scala, Giovanni;
Adair, David;
Ciccone, Carla;
Maruotti, Giuseppe M.;
Martinelli, Pasquale;
Guida, Maurizio

Publication type:

Article

Artificial intelligence, fetal echocardiography, and congenital heart disease.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 6, p. 733, doi. 10.1002/pd.5892

By:

Day, Thomas G.;
Kainz, Bernhard;
Hajnal, Jo;
Razavi, Reza;
Simpson, John M.

Publication type:

Article

Obituary: Bruno Brambati, MD (29 February 1940-3 August 2020).

Published in:

2021

By:

Grati, Francesca Romana;
Simoni, Giuseppe

Publication type:

Editorial

Issue Information.

Published in:: Prenatal Diagnosis, 2021, v. 41, n. 6, p. 649, doi. 10.1002/pd.5743
Publication type:: Article