217 related articles for article (PubMed ID: 22425634)
1. Prenatal diagnosis of a 12q22q23.2 interstitial deletion by array CGH in a malformed fetus.
Kremer V; Girard F; Gasser B; Marcellin L; Christmann D; Nisand I; Schmitt E; Florent S; Flori E
Eur J Med Genet; 2012 Apr; 55(4):269-73. PubMed ID: 22425634
[TBL] [Abstract][Full Text] [Related]
2. De novo 2q36.1q36.3 interstitial deletion involving the PAX3 and EPHA4 genes in a fetus with spina bifida and cleft palate.
Goumy C; Gay-Bellile M; Eymard-Pierre E; Kemeny S; Gouas L; Déchelotte P; Gallot D; Véronèse L; Tchirkov A; Pebrel-Richard C; Vago P
Birth Defects Res A Clin Mol Teratol; 2014 Jun; 100(6):507-11. PubMed ID: 24753315
[TBL] [Abstract][Full Text] [Related]
3. Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization.
Cain CC; Saul D; Attanasio L; Oehler E; Hamosh A; Blakemore K; Stetten G
Prenat Diagn; 2007 Apr; 27(4):373-9. PubMed ID: 17286317
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis and molecular characterization of an interstitial 1q24.3-31.3 deletion: case report and review.
Prontera P; Clerici G; Bernardini L; Schippa M; Capalbo A; Manes I; Giuffrida MG; Barbieri MG; Ardisia C; Donti E
Genet Couns; 2011; 22(1):41-8. PubMed ID: 21614987
[TBL] [Abstract][Full Text] [Related]
5. Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.
Chen CP; Su YN; Chen YY; Chern SR; Liu YP; Wu PC; Lee CC; Chen YT; Wang W
Taiwan J Obstet Gynecol; 2011 Sep; 50(3):345-52. PubMed ID: 22030051
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly.
Courtens W; Tjalma W; Messiaen L; Vamos E; Martin JJ; Van Bogaert E; Keersmaekers G; Meulyzer P; Wauters J
Am J Med Genet; 1998 May; 77(3):188-97. PubMed ID: 9605585
[TBL] [Abstract][Full Text] [Related]
7. Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization.
Cain CC; Saul DO; Oehler E; Blakemore K; Stetten G
Fetal Diagn Ther; 2008; 24(3):286-90. PubMed ID: 18818501
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH).
Hung CC; Lin CH; Lin SY; Shin JC; Lee CN; Su YN
Gene; 2012 Mar; 495(2):178-82. PubMed ID: 22248625
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
[TBL] [Abstract][Full Text] [Related]
10. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.
Law LW; Lau TK; Fung TY; Leung TY; Wang CC; Choy KW
BJOG; 2009 Jan; 116(2):339-43. PubMed ID: 19018765
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.
Sifakis S; Eleftheriades M; Kappou D; Murru R; Konstantinidou A; Orru S; Ziegler M; Liehr T; Manolakos E; Papoulidis I
Birth Defects Res A Clin Mol Teratol; 2014 Apr; 100(4):284-93. PubMed ID: 24677675
[TBL] [Abstract][Full Text] [Related]
12. Prenatally diagnosed de novo segmental amplification or deletion by microarray-based comparative genomic hybridization: A retrospective study.
Peng HH; Lee CH; Su SY; Chen KJ; Lee YC; You SH; Lee WF; Cheng PJ
Taiwan J Obstet Gynecol; 2019 Sep; 58(5):662-666. PubMed ID: 31542089
[TBL] [Abstract][Full Text] [Related]
13. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
[TBL] [Abstract][Full Text] [Related]
14. Prenatal and postnatal findings in a 10.6 Mb interstitial deletion at 10p11.22-p12.31.
Sosoi S; Streata I; Tudorache S; Burada F; Siminel M; Cernea N; Ioana M; Iliescu DG; Mixich F
J Hum Genet; 2015 Apr; 60(4):183-5. PubMed ID: 25652353
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Prenatal diagnosis of a female fetus with ring chromosome 9, 46,XX,r(9)(p24q34), and a de novo interstitial 9p deletion.
Penacho V; Galán F; Martín-Bayón TA; Mayo S; Manchón I; Carrasco A; Martínez-Castellano F; Alcaraz LA
Cytogenet Genome Res; 2014; 144(4):275-9. PubMed ID: 25722017
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Prenatal diagnosis of 2q32 deletion syndrome characterized by multiple segmental deletions and complex chromosomal rearrangement involving chromosomes 2, 5 and 7.
Thorson HL; Surti U; Sathanoori M; Kochmar SJ; Torchia B; Rajkovic A
Fetal Diagn Ther; 2012; 31(3):196-200. PubMed ID: 22415219
[TBL] [Abstract][Full Text] [Related]
19. CGH Array and Karyotype as Complementary Tools in Prenatal Diagnosis: Prenatal Diagnosis of a 4q Derivative Chromosome from Maternal 4q;11q Translocation.
Gonzalez C; Serrano MG; Barbancho Lopez C; Garcia-Riaño T; Barea Calero V; Moreno Perea R; Rodriguez Mogollón B; Queipo Rojas A; Climent AG; Cava Valenciano F
Fetal Pediatr Pathol; 2018 Jun; 37(3):184-190. PubMed ID: 29771170
[TBL] [Abstract][Full Text] [Related]
20. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.
Lee CN; Lin SY; Lin CH; Shih JC; Lin TH; Su YN
BJOG; 2012 Apr; 119(5):614-25. PubMed ID: 22313859
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]