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.
137 related articles for article (PubMed ID: 31055824)
1. [Prenatal diagnosis of a fetus with trisomies of 11q23.3q25 and 22q11.1q11.21]. Li F; Tang J; Xie X; Tang S; Wu A; Tang Q; Tan W; Guo X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Jun; 36(6):632-635. PubMed ID: 31055824 [TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of supernumerary der(22)t(11;22) associated with the Dandy-Walker malformation in a fetus. Chen CP; Liu FF; Jan SW; Yang YC; Lan CC Prenat Diagn; 1996 Dec; 16(12):1137-40. PubMed ID: 8994250 [TBL] [Abstract][Full Text] [Related]
3. [Genetic diagnosis and follow up of a fetus with Emanuel syndrome]. Zhao Y; Pang H; Gao M; Feng X; Guan Y; Zhao H; Tong D; Hua J; Cao X; He S; Li-Ling J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):709-713. PubMed ID: 28981939 [TBL] [Abstract][Full Text] [Related]
4. [Genetic diagnosis of a fetus with Dandy-Walker syndrome]. Luo Y; Sun Y; Qian Y; Shen M; Wang L; Jin F; Dong M Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jan; 37(1):8-11. PubMed ID: 31922586 [TBL] [Abstract][Full Text] [Related]
5. [Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array]. Shi S; Pan G; Yang Y; Yan R; Li W Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):195-9. PubMed ID: 27060314 [TBL] [Abstract][Full Text] [Related]
6. Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center. Lau TK; Cheung SW; Lo PS; Pursley AN; Chan MK; Jiang F; Zhang H; Wang W; Jong LF; Yuen OK; Chan HY; Chan WS; Choy KW Ultrasound Obstet Gynecol; 2014 Mar; 43(3):254-64. PubMed ID: 24339153 [TBL] [Abstract][Full Text] [Related]
7. [Diagnosis of a fetus with partial 17p trisomy using chromosomal microarray analysis]. Zhao L; Wan B Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):488-490. PubMed ID: 31030440 [TBL] [Abstract][Full Text] [Related]
8. [Prenatal diagnosis of partial trisomy 3q in a fetus]. Su N; Lou G; Wang H; Hao B; Liao S Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug; 36(8):813-816. PubMed ID: 31400135 [TBL] [Abstract][Full Text] [Related]
9. [Genetic analysis of a fetus with partial 1q monosomy and partial 17q trisomy]. Lin S; Zhang Z; Wu J; Ji Y; Fang Q; Chen B; Zhou Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):340-3. PubMed ID: 27264817 [TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of partial trisomy 22 derived from a maternal t(11; 22) (q23; q11). Sou S; Takabayashi T; Sasaki H; Sasamoto K; Shintaku Y; Li ZJ; Ozawa N; Yajima A Tohoku J Exp Med; 1987 Dec; 153(4):389-93. PubMed ID: 3441929 [TBL] [Abstract][Full Text] [Related]
11. [Prenatal diagnosis and genetic analysis of a fetus with der(X)t(X;Y)(p22.3;q11.2)]. Li J; Dong Y; Li J; Luo J; Li C; Qi H Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1287-1290. PubMed ID: 33179242 [TBL] [Abstract][Full Text] [Related]
12. [Prenatal diagnosis of a fetus with partial trisomy 8p resulting from a balanced maternal translocation by array-based comparative genomic hybridization]. Guo C; Wang J; Zhao L; Liu J; Wang J; Xiao J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):375-7. PubMed ID: 26037354 [TBL] [Abstract][Full Text] [Related]
13. [Genetic study of a fetus with 9p direct duplication deletion syndrome]. Shi S; Lin S; Lou X; Li W Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):419-422. PubMed ID: 28604969 [TBL] [Abstract][Full Text] [Related]
14. [Diagnosis of a fetus with a de novo 16q partial trisomy syndrome]. Hu L; Wang W; Li H; Zhou S; Liu S; Yang M; Bu X; He J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1084-1086. PubMed ID: 32924106 [TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings. Aslan H; Karaman B; Yildirim G; Ceylan Y Prenat Diagn; 2005 Nov; 25(11):1024-7. PubMed ID: 16231308 [TBL] [Abstract][Full Text] [Related]
16. [Prenatal genetic analysis of three fetuses with abnormalities of chromosome 22]. Ge Y; Zhang J; Cai M; Chen X; Zhou Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):405-409. PubMed ID: 32219823 [TBL] [Abstract][Full Text] [Related]
17. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation. Hou JW Chang Gung Med J; 2003 Jan; 26(1):48-52. PubMed ID: 12656309 [TBL] [Abstract][Full Text] [Related]
19. Non-invasive prenatal screening for Emanuel syndrome. Luo Y; Lin J; Sun Y; Qian Y; Wang L; Chen M; Dong M; Jin F Mol Cytogenet; 2020; 13():9. PubMed ID: 32158503 [TBL] [Abstract][Full Text] [Related]
20. Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11). Fryns JP; Kleczkowska A Ann Genet; 1987; 30(2):109-10. PubMed ID: 3499841 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]