154 related articles for article (PubMed ID: 35140290)
1. Frequency and clinical significance of chromosomal inversions prenatally diagnosed by second trimester amniocentesis.
Chien CW; Chao AS; Chang YL; Chen KJ; Peng HH; Lin YT; Chao A; Chang SD
Sci Rep; 2022 Feb; 12(1):2215. PubMed ID: 35140290
[TBL] [Abstract][Full Text] [Related]
2. Prenatally diagnosed balanced chromosome rearrangements: eight years' experience.
Peng HH; Chao AS; Wang TH; Chang YL; Chang SD
J Reprod Med; 2006 Sep; 51(9):699-703. PubMed ID: 17039698
[TBL] [Abstract][Full Text] [Related]
3. Pattern of chromosomal inversions identified by a birth defects registry, Hawaii, 1986-2002.
Forrester MB; Merz RD
Congenit Anom (Kyoto); 2007 Sep; 47(3):97-100. PubMed ID: 17688468
[TBL] [Abstract][Full Text] [Related]
4. [Study on key techniques and intervention in reducing birth defects].
Zhu BS; Su J; Lu XH; He J; Zhu S; Jiao CX; Zhang JM; Tang XH; Tao Y; Lin KP; Chen H; Li SY
Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):658-63. PubMed ID: 22176989
[TBL] [Abstract][Full Text] [Related]
5. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M
Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
[TBL] [Abstract][Full Text] [Related]
6. The application of late amniocentesis: a retrospective study in a tertiary fetal medicine center in China.
Li Y; Yan H; Chen J; Chen F; Jian W; Wang J; Ye X; Li Y; Li N; Chiu PCN; Chen M
BMC Pregnancy Childbirth; 2021 Mar; 21(1):266. PubMed ID: 33784964
[TBL] [Abstract][Full Text] [Related]
7. Society for Maternal-Fetal Medicine Consult Series #57: Evaluation and management of isolated soft ultrasound markers for aneuploidy in the second trimester: (Replaces Consults #10, Single umbilical artery, October 2010; #16, Isolated echogenic bowel diagnosed on second-trimester ultrasound, August 2011; #17, Evaluation and management of isolated renal pelviectasis on second-trimester ultrasound, December 2011; #25, Isolated fetal choroid plexus cysts, April 2013; #27, Isolated echogenic intracardiac focus, August 2013).
; Prabhu M; Kuller JA; Biggio JR
Am J Obstet Gynecol; 2021 Oct; 225(4):B2-B15. PubMed ID: 34171388
[TBL] [Abstract][Full Text] [Related]
8. Evaluation of prenatally diagnosed structural congenital anomalies.
Gagnon A;
J Obstet Gynaecol Can; 2009 Sep; 31(9):875-881. PubMed ID: 19941713
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis and outcome of pregnancy in 2036 women investigated by amniocentesis.
Squire JA; Nauth L; Ridler MA; Sutton S; Timberlake C
Hum Genet; 1982; 61(3):215-22. PubMed ID: 7173865
[TBL] [Abstract][Full Text] [Related]
10. [Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].
Guo YL; Wang L; Xue SW; Qu SZ; Yang J; Xu H; Bai ZX; Liu N; Kong XD
Zhonghua Fu Chan Ke Za Zhi; 2018 Jul; 53(7):464-470. PubMed ID: 30078256
[No Abstract] [Full Text] [Related]
11. Paracentric inversions in humans: a review of 446 paracentric inversions with presentation of 120 new cases.
Pettenati MJ; Rao PN; Phelan MC; Grass F; Rao KW; Cosper P; Carroll AJ; Elder F; Smith JL; Higgins MD
Am J Med Genet; 1995 Jan; 55(2):171-87. PubMed ID: 7717416
[TBL] [Abstract][Full Text] [Related]
12. PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13).
Yakut S; Cetin Z; Sanhal C; Karaman B; Mendilcioglu I; Karauzum SB
Genet Couns; 2015; 26(2):243-7. PubMed ID: 26349196
[TBL] [Abstract][Full Text] [Related]
13. The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal age.
Hagen A; Entezami M; Gasiorek-Wiens A; Albig M; Becker R; Knoll U; Stumm M; Wegner RD
Ultraschall Med; 2011 Jun; 32(3):302-6. PubMed ID: 20972947
[TBL] [Abstract][Full Text] [Related]
14. Clinical and cytogenetic results of a series of amniocentesis cases from Northeast China: a report of 2500 cases.
An N; Li LL; Wang RX; Li LL; Yue JM; Liu RZ
Genet Mol Res; 2015 Dec; 14(4):15660-7. PubMed ID: 26634534
[TBL] [Abstract][Full Text] [Related]
15. Patterns of chromosomal deletions identified by a birth defects registry, Hawaii, 1986-2003.
Forrester MB; Merz RD
Congenit Anom (Kyoto); 2007 Jun; 47(2):58-62. PubMed ID: 17504388
[TBL] [Abstract][Full Text] [Related]
16. Evaluation of clinical and cytogenetic findings on 1,068 second-trimester amniocenteses in Southeast Turkey.
Balkan M; Akbas H; Kalkanli S; Sakar MN; Fidanboy M; Alp MN; Budak T
Clin Exp Obstet Gynecol; 2011; 38(4):364-8. PubMed ID: 22268276
[TBL] [Abstract][Full Text] [Related]
17. [Clinical features of abnormal chromosome karyotypes in twin pregnancies complicated with structural abnormalities].
Zhong SL; Fang Q; Chen BJ; Han ZY; Luo YM; Chen JS; Xie YJ
Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):649-54. PubMed ID: 22176987
[TBL] [Abstract][Full Text] [Related]
18. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.
Daniel A; Hook EB; Wulf G
Am J Med Genet; 1989 May; 33(1):14-53. PubMed ID: 2750783
[TBL] [Abstract][Full Text] [Related]
19. Prenatal screening for fetal aneuploidy in singleton pregnancies.
Chitayat D; Langlois S; Douglas Wilson R; ;
J Obstet Gynaecol Can; 2011 Jul; 33(7):736-750. PubMed ID: 21749752
[TBL] [Abstract][Full Text] [Related]
20. Population-based trends in invasive prenatal diagnosis for ultrasound-based indications: two decades of change from 1994 to 2016.
Lostchuck E; Poulton A; Halliday J; Hui L
Ultrasound Obstet Gynecol; 2019 Apr; 53(4):503-511. PubMed ID: 29877030
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
