266 related articles for article (PubMed ID: 23232358)
1. Prenatal diagnosis of de novo partial trisomy 18p and partial monosomy 18q recurrent in a family with fatal aortic coarctation.
Hu H; Hao J; Yao H; Chang Q; Li R; Zhang X; Liang Z
Gene; 2013 Mar; 517(1):132-6. PubMed ID: 23232358
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.
Chen CP; Chen YY; Chern SR; Wu PS; Su JW; Chen YT; Chen LF; Wang W
Gene; 2013 Mar; 516(1):138-42. PubMed ID: 23266815
[TBL] [Abstract][Full Text] [Related]
3. De novo partial trisomy 18p and partial monosomy 18q in a patient with anorectal malformation.
Bartels E; Draaken M; Kazmierczak B; Spranger S; Schramm C; Baudisch F; Nöthen MM; Schmiedeke E; Ludwig M; Reutter H
Cytogenet Genome Res; 2011; 134(3):243-8. PubMed ID: 21709416
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
5. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.
Prabhakara K; Wyandt HE; Huang XL; Prasad KS; Ramadevi AR
Ann Genet; 2004; 47(3):297-303. PubMed ID: 15337476
[TBL] [Abstract][Full Text] [Related]
6. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.
Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Hsu CY; Wu PC; Town DD; Lee DJ; Ma GC; Wang W
Taiwan J Obstet Gynecol; 2010 Sep; 49(3):320-6. PubMed ID: 21056318
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies.
Lee MJ; Park SH; Shim SH; Moon MJ; Cha DH
Taiwan J Obstet Gynecol; 2019 May; 58(3):318-323. PubMed ID: 31122516
[TBL] [Abstract][Full Text] [Related]
12. Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings.
Shojaei A; Behjati F; Derakhshandeh-Peykar P; Razzaghy-Azar M; Otukesh H; Kariminejad R; Dowlati MA; Rashidi-Nezhad A; Tavakkoly-Bazzaz J
Gene; 2013 Mar; 517(1):137-45. PubMed ID: 23201896
[TBL] [Abstract][Full Text] [Related]
13. Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH.
Choy KW; Chan LW; Tang MH; Ng LK; Leung TY; Lau TK
J Matern Fetal Neonatal Med; 2009 Nov; 22(11):1014-20. PubMed ID: 19900039
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
15. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Chern SR; Lee CC; Chen YJ; Wang W
Prenat Diagn; 2005 Dec; 25(12):1170-2. PubMed ID: 16315335
[No Abstract] [Full Text] [Related]
16. Two-Generation Transmission of Trisomy 18p: Prenatal Diagnosis in a Woman with Mild Intellectual Disability.
Yu Y; Jiang Y; Hu X; Zhang H; Liu R; Wang R
Cytogenet Genome Res; 2019; 157(4):220-226. PubMed ID: 30939474
[TBL] [Abstract][Full Text] [Related]
17. Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature.
Schmidt B; Udink ten Cate F; Weiss M; Koehler U
Eur J Pediatr; 2012 Jul; 171(7):1047-53. PubMed ID: 22302461
[TBL] [Abstract][Full Text] [Related]
18. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
[TBL] [Abstract][Full Text] [Related]
19. [Genotypic and phenotypic analysis of a patient with de novo partial monosomy 18p and partial trisomy 18q].
Xiao B; Ji X; Ye H; Liu Y; Cao Y; Sun Y; Wei W; Qiu W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):484-487. PubMed ID: 31030439
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of pure partial monosomy 18p associated with holoprosencephaly and congenital heart defects.
Yi Z; Yingjun X; Yongzhen C; Liangying Z; Meijiao S; Baojiang C
Gene; 2014 Jan; 533(2):565-9. PubMed ID: 24091065
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
