These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 33550297)

  • 1. The Diagnostic Yield of Prenatal Genetic Technologies in Congenital Heart Disease: A Prospective Cohort Study.
    Mone F; Stott BK; Hamilton S; Seale AN; Quinlan-Jones E; Allen S; Hurles ME; McMullan DJ; Maher ER; Kilby MD
    Fetal Diagn Ther; 2021 Feb; ():1-8. PubMed ID: 33550297
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Incremental yield of whole-genome sequencing over chromosomal microarray analysis and exome sequencing for congenital anomalies in prenatal period and infancy: systematic review and meta-analysis.
    Shreeve N; Sproule C; Choy KW; Dong Z; Gajewska-Knapik K; Kilby MD; Mone F
    Ultrasound Obstet Gynecol; 2024 Jan; 63(1):15-23. PubMed ID: 37725747
    [TBL] [Abstract][Full Text] [Related]  

  • 3. COngenital heart disease and the Diagnostic yield with Exome sequencing (CODE) study: prospective cohort study and systematic review.
    Mone F; Eberhardt RY; Morris RK; Hurles ME; McMullan DJ; Maher ER; Lord J; Chitty LS; Giordano JL; Wapner RJ; Kilby MD;
    Ultrasound Obstet Gynecol; 2021 Jan; 57(1):43-51. PubMed ID: 32388881
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect.
    Qiao F; Wang Y; Zhang C; Zhou R; Wu Y; Wang C; Meng L; Mao P; Cheng Q; Luo C; Hu P; Xu Z
    Ultrasound Obstet Gynecol; 2021 Sep; 58(3):377-387. PubMed ID: 33142350
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies.
    Vaseghi P; Habibi L; Neidich JA; Cao Y; Fattahi N; Rashidi-Nezhad R; Salehnezhad T; Dalili H; Rahimi Sharbaf F; Zarkesh MR; Malekian M; Mokhberdezfuli M; Mehrtash A; Ardeshirdavani A; Kariminejad R; Ghorbansabagh V; Sadeghimoghadam P; Naddaf A; Esmaeilnia Shirvany T; Mosayebi Z; Sahebdel B; Golshahi F; Shirazi M; Shamel S; Moeini R; Heidari A; Daneshmand MA; Ghasemi R; Akrami SM; Rashidi-Nezhad A
    Eur J Hum Genet; 2024 Jan; ():. PubMed ID: 38278869
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis.
    Mone F; Eberhardt RY; Hurles ME; Mcmullan DJ; Maher ER; Lord J; Chitty LS; Dempsey E; Homfray T; Giordano JL; Wapner RJ; Sun L; Sparks TN; Norton ME; Kilby MD
    Ultrasound Obstet Gynecol; 2021 Oct; 58(4):509-518. PubMed ID: 33847422
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis for fetuses with isolated and non-isolated congenital heart defects using chromosomal microarray and exome sequencing.
    Xing Y; Zhang Y; Chen J; Wu F; Yuan M; Zou G; Yang Y; Zhou F; Zhou J; Sun L
    Prenat Diagn; 2022 Jun; 42(7):873-880. PubMed ID: 35584285
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting.
    Yi T; Hao X; Sun H; Zhang Y; Han J; Gu X; Sun L; Liu X; Zhao Y; Guo Y; Zhou X; He Y
    ESC Heart Fail; 2023 Apr; 10(2):917-930. PubMed ID: 36478645
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Yield rate of chromosomal microarray analysis in fetuses with congenital heart defects.
    Turan S; Asoglu MR; Gabbay-Benziv R; Doyle L; Harman C; Turan OM
    Eur J Obstet Gynecol Reprod Biol; 2018 Feb; 221():172-176. PubMed ID: 29306563
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes.
    Al-Hamed MH; Kurdi W; Khan R; Tulbah M; AlNemer M; AlSahan N; AlMugbel M; Rafiullah R; Assoum M; Monies D; Shah Z; Rahbeeni Z; Derar N; Hakami F; Almutairi G; AlOtaibi A; Ali W; AlShammasi A; AlMubarak W; AlDawoud S; AlAmri S; Saeed B; Bukhari H; Ali M; Akili R; Alquayt L; Hagos S; Elbardisy H; Akilan A; Almuhana N; AlKhalifah A; Abouelhoda M; Ramzan K; Sayer JA; Imtiaz F
    Hum Genet; 2022 Jan; 141(1):101-126. PubMed ID: 34853893
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis.
    Sukenik-Halevy R; Sukenik S; Koifman A; Alpert Y; Hershkovitz R; Levi A; Biron-Shental T
    Prenat Diagn; 2016 Dec; 36(13):1185-1191. PubMed ID: 27794172
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnostic yield of exome sequencing in prenatal agenesis of corpus callosum: systematic review and meta-analysis.
    Mustafa HJ; Barbera JP; Sambatur EV; Pagani G; Yaron Y; Baptiste CD; Wapner RJ; Brewer CJ; Khalil A
    Ultrasound Obstet Gynecol; 2024 Mar; 63(3):312-320. PubMed ID: 37519216
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
    Geng J; Picker J; Zheng Z; Zhang X; Wang J; Hisama F; Brown DW; Mullen MP; Harris D; Stoler J; Seman A; Miller DT; Fu Q; Roberts AE; Shen Y
    BMC Genomics; 2014 Dec; 15(1):1127. PubMed ID: 25516202
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital heart defects and copy number variants associated with neurodevelopmental impairment.
    Findley TO; Crain AK; Mahajan S; Deniwar A; Davis J; Solis Zavala AS; Corno AF; Rodriguez-Buritica D
    Am J Med Genet A; 2022 Jan; 188(1):13-23. PubMed ID: 34472185
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal genetic diagnosis associated with fetal ventricular septal defect: an assessment based on chromosomal microarray analysis and exome sequencing.
    Wang Y; Li R; Fu F; Huang R; Li D; Liao C
    Front Genet; 2023; 14():1260995. PubMed ID: 38075692
    [No Abstract]   [Full Text] [Related]  

  • 16. Exome sequencing as first-tier test for fetuses with severe central nervous system structural anomalies.
    Yaron Y; Ofen Glassner V; Mory A; Zunz Henig N; Kurolap A; Bar Shira A; Brabbing Goldstein D; Marom D; Ben Sira L; Baris Feldman H; Malinger G; Krajden Haratz K; Reches A
    Ultrasound Obstet Gynecol; 2022 Jul; 60(1):59-67. PubMed ID: 35229910
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China.
    Zhou Y; Lu X; Zhang Y; Ge Y; Xu Y; Wu L; Jiang Y
    Cytogenet Genome Res; 2022; 162(7):354-364. PubMed ID: 36907182
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Estimating the frequency of causal genetic variants in foetuses with congenital heart defects: a Chinese cohort study.
    Lu F; Xue P; Zhang B; Wang J; Yu B; Liu J
    Orphanet J Rare Dis; 2022 Jan; 17(1):2. PubMed ID: 34983622
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].
    Wu X; Fu F; Li R; Pan M; Han J; Zhen L; Yang X; Zhang Y; Li F; Liao C
    Zhonghua Fu Chan Ke Za Zhi; 2014 Dec; 49(12):893-8. PubMed ID: 25608988
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of fetuses with increased nuchal translucency using an approach based on quantitative fluorescent polymerase chain reaction and genomic microarray.
    Pan M; Han J; Zhen L; Yang X; Li R; Liao C; Li DZ
    Eur J Obstet Gynecol Reprod Biol; 2016 Feb; 197():164-7. PubMed ID: 26771907
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.