OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center
Tuğba Saraç Sivrikoz, Seher Başaran, Recep Has, et al.
Archives of Gynecology and Obstetrics (2021) Vol. 305, Iss. 2, pp. 323-342
Closed Access | Times Cited: 9
Tuğba Saraç Sivrikoz, Seher Başaran, Recep Has, et al.
Archives of Gynecology and Obstetrics (2021) Vol. 305, Iss. 2, pp. 323-342
Closed Access | Times Cited: 9
Showing 9 citing articles:
Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology
Ferdinand Dhombres, Patricia Morgan, Bimal P. Chaudhari, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 2, pp. 231-242
Open Access | Times Cited: 37
Ferdinand Dhombres, Patricia Morgan, Bimal P. Chaudhari, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 2, pp. 231-242
Open Access | Times Cited: 37
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, et al.
Genes (2023) Vol. 14, Iss. 1, pp. 160-160
Open Access | Times Cited: 22
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, et al.
Genes (2023) Vol. 14, Iss. 1, pp. 160-160
Open Access | Times Cited: 22
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation
Elizabeth Goldmuntz, Anne S. Bassett, Erik Boot, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 6-7, pp. 804-814
Open Access | Times Cited: 2
Elizabeth Goldmuntz, Anne S. Bassett, Erik Boot, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 6-7, pp. 804-814
Open Access | Times Cited: 2
Prenatal sonographic findings in a cohort of foetuses with a confirmed 22q11.2 microdeletion at a single Chinese Tertiary Centre
Xiangyi Jing, Yongling Zhang, Zhen Li, et al.
Journal of Obstetrics and Gynaecology (2022) Vol. 42, Iss. 7, pp. 2935-2940
Closed Access | Times Cited: 6
Xiangyi Jing, Yongling Zhang, Zhen Li, et al.
Journal of Obstetrics and Gynaecology (2022) Vol. 42, Iss. 7, pp. 2935-2940
Closed Access | Times Cited: 6
Decoding 22q11.2: prenatal profiling and first‐trimester risk assessment in Danish nationwide cohort
Kasper Gadsbøll, Ida Vogel, Lars Henning Pedersen, et al.
Ultrasound in Obstetrics and Gynecology (2023) Vol. 63, Iss. 1, pp. 34-43
Open Access | Times Cited: 3
Kasper Gadsbøll, Ida Vogel, Lars Henning Pedersen, et al.
Ultrasound in Obstetrics and Gynecology (2023) Vol. 63, Iss. 1, pp. 34-43
Open Access | Times Cited: 3
Isolated polyhydramnios: Is a genetic evaluation of value?
Xiao‐Mei Lin, Zhen Li, Yun‐Jing Wen, et al.
European Journal of Obstetrics & Gynecology and Reproductive Biology (2023) Vol. 293, pp. 115-118
Closed Access | Times Cited: 2
Xiao‐Mei Lin, Zhen Li, Yun‐Jing Wen, et al.
European Journal of Obstetrics & Gynecology and Reproductive Biology (2023) Vol. 293, pp. 115-118
Closed Access | Times Cited: 2
Prenatal diagnosis, ultrasound findings, and pregnancy outcome of 17q12 deletion and duplication syndromes: a retrospective case series
Xiaojin Luo, Xiaohang Chen, Xiaoyi Cong, et al.
Archives of Gynecology and Obstetrics (2024)
Closed Access
Xiaojin Luo, Xiaohang Chen, Xiaoyi Cong, et al.
Archives of Gynecology and Obstetrics (2024)
Closed Access
Clinical Course and Outcome of Prenatally Detected 22q11.2 Deletion Syndrome—A Retrospective Analysis
Chiara Paternostro, Stephanie Springer, Gregor Kasprian, et al.
Diagnostics (2023) Vol. 13, Iss. 13, pp. 2244-2244
Open Access | Times Cited: 1
Chiara Paternostro, Stephanie Springer, Gregor Kasprian, et al.
Diagnostics (2023) Vol. 13, Iss. 13, pp. 2244-2244
Open Access | Times Cited: 1
The Effectiveness of Chromosomal Microarray Analysis in Diagnosis of Fetuses with Cardiac Anomalies: Cohort Research
Hilal ŞENTÜRK, Bilge ÖZSAİT SELÇUK, Tuğba Saraç Sivrikoz, et al.
Turkiye Klinikleri Journal of Medical Sciences (2023) Vol. 43, Iss. 3, pp. 302-313
Open Access
Hilal ŞENTÜRK, Bilge ÖZSAİT SELÇUK, Tuğba Saraç Sivrikoz, et al.
Turkiye Klinikleri Journal of Medical Sciences (2023) Vol. 43, Iss. 3, pp. 302-313
Open Access
