165 related articles for article (PubMed ID: 30910156)
41. Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound.
Chen CP; Wang LK; Wu PC; Chang TY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2017 Feb; 56(1):102-105. PubMed ID: 28254208
[TBL] [Abstract][Full Text] [Related]
42. Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).
Chen CP; Lin YH; Au HK; Su YN; Hsu CY; Liu YP; Wu PC; Chern SR; Chen YT; Chen LF; Hsieh AH; Wang W
Taiwan J Obstet Gynecol; 2011 Sep; 50(3):359-65. PubMed ID: 22030053
[TBL] [Abstract][Full Text] [Related]
43. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
Chen CP; Su YN; Hsu CY; Chern SR; Lee CC; Chen YT; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322
[TBL] [Abstract][Full Text] [Related]
44. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry.
Chen CP; Su YN; Lin SP; Chern SR; Su JW; Chen YT; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2013 Mar; 52(1):120-4. PubMed ID: 23548232
[TBL] [Abstract][Full Text] [Related]
45. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry.
Chen CP; Hwang KS; Su HY; Lin SP; Su YN; Chern SR; Su JW; Chen YT; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2013 Mar; 52(1):125-8. PubMed ID: 23548233
[TBL] [Abstract][Full Text] [Related]
46. Molecular cytogenetic analysis of a de novo 5q31q33 deletion associated multiple congenital anomalies: case report.
Kramer RL; Feldman B; Ebrahim SA; Kasperski SB; Johnson MP; Evans MI
Am J Med Genet; 1999 Jan; 82(2):143-5. PubMed ID: 9934978
[TBL] [Abstract][Full Text] [Related]
47. De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: prenatal diagnosis and molecular cytogenetic characterization.
Chen CP; Fu CH; Chern SR; Wu PS; Su JW; Lee CC; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2013 Sep; 52(3):401-6. PubMed ID: 24075381
[TBL] [Abstract][Full Text] [Related]
48. Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound.
Chen CP; Chang SY; Lin CJ; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen WL; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2018 Oct; 57(5):734-738. PubMed ID: 30342662
[TBL] [Abstract][Full Text] [Related]
49. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
Dietze I; Fritz B; Huhle D; Simoens W; Piecha E; Rehder H
Fetal Diagn Ther; 2004; 19(3):251-60. PubMed ID: 15067236
[TBL] [Abstract][Full Text] [Related]
50. Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.
Chen CP; Chang SY; Chen YN; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2018 Oct; 57(5):739-744. PubMed ID: 30342663
[TBL] [Abstract][Full Text] [Related]
51. Prenatal diagnosis of de novo interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the long bones.
Chen CP; Chern SR; Lee CC; Chen LF; Chuang CY
Prenat Diagn; 1998 May; 18(5):490-5. PubMed ID: 9621384
[TBL] [Abstract][Full Text] [Related]
52. Identification of a Novel Heterozygous
Riedhammer KM; Siegel C; Alhaddad B; Montoya C; Kovacs-Nagy R; Wagner M; Meitinger T; Hoefele J
Front Pediatr; 2017; 5():251. PubMed ID: 29226118
[TBL] [Abstract][Full Text] [Related]
53. Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review.
Chen CP; Su YN; Chen CY; Chern SR; Wu PS; Su JW; Lee CC; Chen LF; Wang W
Genomics; 2013 Oct; 102(4):265-9. PubMed ID: 23981964
[TBL] [Abstract][Full Text] [Related]
54. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1).
Chen CP; Chang SJ; Chern SR; Wu PS; Chen YT; Su JW; Chen WL; Wang W
Gene; 2013 Jun; 521(2):311-5. PubMed ID: 23545313
[TBL] [Abstract][Full Text] [Related]
55. Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses.
Tuğ E; Karcaaltincaba D; Yirmibeş Karaoğuz M; Saat H; Özek A
J Matern Fetal Neonatal Med; 2017 Jul; 30(13):1579-1583. PubMed ID: 27431726
[TBL] [Abstract][Full Text] [Related]
56. Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise.
Chen CP; Chern SR; Chen YY; Wu PC; Town DD; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):430-4. PubMed ID: 23040931
[TBL] [Abstract][Full Text] [Related]
57. Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities.
Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2018 Feb; 57(1):128-132. PubMed ID: 29458882
[TBL] [Abstract][Full Text] [Related]
58. Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3.
Christopoulou G; Tzetis M; Konstantinidou AE; Tsezou A; Kanavakis E; Kitsiou-Tzeli S; Velissariou V
Eur J Med Genet; 2012 Jan; 55(1):75-9. PubMed ID: 21914491
[TBL] [Abstract][Full Text] [Related]
59. Prenatal diagnosis of de novo interstitial 2q14.2-2q21.3 deletion assisted by array-based comparative genomic hybridization: a case report.
Peng HH; Wang CJ; Wang TH; Chang SD
J Reprod Med; 2006 May; 51(5):438-42. PubMed ID: 16779995
[TBL] [Abstract][Full Text] [Related]
60. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
