Prenatal exome sequencing - facing uncertainty

被引:0
作者
Borrell, Antoni [1 ]
机构
[1] BCNatal Hosp Clin, Barcelona, Spain
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
S22.1
引用
收藏
页码:86 / 86
页数:1
相关论文
共 50 条
[21]   Prenatal exome sequencing: A useful tool for the fetal neurologist [J].
de Koning, Maayke A. ;
Hoffer, Mariette J., V ;
Nibbeling, Esther A. R. ;
Bijlsma, Emilia K. ;
Toirkens, Menno J. P. ;
Adama-Scheltema, Phebe N. ;
Verweij, E. Joanne ;
Veenhof, Marieke B. ;
Santen, Gijs W. E. ;
Peeters-Scholte, Cacha M. P. C. D. .
CLINICAL GENETICS, 2022, 101 (01) :65-77
[22]   Patient perspectives on the utility and impact of prenatal exome sequencing [J].
Swanson, Kate ;
Sahin-Hodoglugil, Nuriye ;
Sparks, Teresa N. ;
Ackerman, Sara ;
Lianoglou, Billie R. ;
Downum, Sarah L. ;
Norton, Mary E. .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2023, 228 (01) :S48-S49
[23]   Importance of complete phenotyping in prenatal whole exome sequencing [J].
Mahmoud Aarabi ;
Olivia Sniezek ;
Huaiyang Jiang ;
Devereux N. Saller ;
Daniel Bellissimo ;
Svetlana A. Yatsenko ;
Aleksandar Rajkovic .
Human Genetics, 2018, 137 :175-181
[24]   Considerations for whole exome sequencing unique to prenatal care [J].
Abou Tayoun, Ahmad ;
Mason-Suares, Heather .
HUMAN GENETICS, 2020, 139 (09) :1149-1159
[25]   Comprehensive prenatal diagnostics: Exome versus genome sequencing [J].
Miceikaite, Ieva ;
Fagerberg, Christina ;
Brasch-Andersen, Charlotte ;
Torring, Pernille Mathiesen ;
Kristiansen, Britta Schlott ;
Hao, Qin ;
Sperling, Lene ;
Ibsen, Mette Holm ;
Loser, Katrin ;
Bendsen, Eske Alf ;
Ousager, Lilian Bomme ;
Larsen, Martin Jakob .
PRENATAL DIAGNOSIS, 2023, 43 (09) :1132-1141
[26]   Implementation of Exome Sequencing in Prenatal Diagnostics: Chances and Challenges [J].
Janicki, Ewa ;
De Rademaeker, Marjan ;
Meunier, Colombine ;
Boeckx, Nele ;
Blaumeiser, Bettina ;
Janssens, Katrien .
DIAGNOSTICS, 2023, 13 (05)
[27]   Use of prenatal exome sequencing in fetuses with ultrasound anomalies [J].
Segura-Puimedon, M. ;
Campos, B. ;
Luna, J. ;
Sintas, C. ;
de Castro-Miro, M. ;
Diez, H. ;
Estruch, S. B. ;
Garcia, R. ;
Quintana, L. ;
Rodriguez, J. ;
Armengol, L. .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) :150-151
[28]   Use of prenatal exome sequencing in fetuses with ultrasound anomalies [J].
Segura-Puimedon, M. ;
Rodriguez-Santiago, B. ;
Vallmajo, A. ;
Codina-Sola, M. ;
Campos, B. ;
Datta, D. ;
Banchs, I. ;
Mattlin, H. ;
Sarria, Y. ;
Abad, O. ;
Rodriguez, J. ;
Perez-Jurado, L. ;
Armengol, L. .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 :11-12
[29]   Prenatal exome and genome sequencing for fetal structural abnormalities [J].
Vora, Neeta L. ;
Norton, Mary E. .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2023, 228 (02) :140-149
[30]   Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities [J].
Drury, Suzanne ;
Williams, Hywel ;
Trump, Natalie ;
Boustred, Christopher ;
Lench, Nicholas ;
Scott, Richard H. ;
Chitty, Lyn S. .
PRENATAL DIAGNOSIS, 2015, 35 (10) :1010-1017