182 related articles for article (PubMed ID: 2410900)
1. Prenatal diagnosis and fetal pathology of partial trisomy 20P-monosomy 4P resulting from paternal translocation.
Vamos E; Pratola D; Van Regemorter N; Freund M; Flament-Durand J; Rodesch F
Prenat Diagn; 1985; 5(3):209-14. PubMed ID: 2410900
[TBL] [Abstract][Full Text] [Related]
2. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
[TBL] [Abstract][Full Text] [Related]
3. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).
Kohlschmidt N; Zielinski J; Brude E; Schäfer D; Olert J; Hallermann C; Coerdt W; Arnemann J
Prenat Diagn; 2000 Feb; 20(2):152-5. PubMed ID: 10694689
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Trisomy 4p and deletion 4p- in a family having translocation, t(4p-; 12p+).
Mortimer JG; Chewings W; Miethke P; Smith GF
Hum Hered; 1978; 28(2):132-40. PubMed ID: 621087
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of der(11)t(11;18)(q24;q21.3) due to paternal balanced translocation and both parents are carriers of alpha-thalassemia-1--a case report.
Chao MC; Yang SY; Chang Y; Huang YW; Liu TC; Lee JP; Chen BH
Kaohsiung J Med Sci; 2001 Aug; 17(8):430-6. PubMed ID: 11715843
[TBL] [Abstract][Full Text] [Related]
8. De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia.
Chen CP; Chern SR; Lee CC; Chen WL; Chen MH; Chang KM
J Med Genet; 1998 Dec; 35(12):1050-3. PubMed ID: 9863609
[TBL] [Abstract][Full Text] [Related]
9. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
Chen CP; Su YN; Chen YY; Su JW; Chern SR; Chen YT; Chen WL; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization.
Chen CP; Su YN; Young RS; Tsai FJ; Wu PC; Chern SR; Town DD; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):506-12. PubMed ID: 21199755
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21.
Lee C; Fowler DJ; Lemyre E; Sandstrom MM; Holmes LB; Morton CC
Am J Med Genet; 2001 May; 100(3):246-50. PubMed ID: 11343311
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of a fetus with partial monosomy 7(q34-->qter) and partial trisomy 18(q21-->qter).
Pluchon E; Giovangrandi Y; Labbe F; Le Bris MJ; Collet M; Brettes JP; Riviere D; Riviere MR
Prenat Diagn; 1993 Oct; 13(10):983-8. PubMed ID: 8309904
[TBL] [Abstract][Full Text] [Related]
14. Duplication 4p and deletion 4p (Wolf-Hirschhorn syndrome) due to complementary gametes from a 3:1 segregation of a maternal balanced t(4;13)(p16;q11) translocation.
Takeno SS; Corbani M; Andrade JA; Smith Mde A; Brunoni D; Melaragno MI
Am J Med Genet A; 2004 Aug; 129A(2):180-3. PubMed ID: 15316961
[TBL] [Abstract][Full Text] [Related]
15. An infant with trisomy 9 mosaicism presenting as a complete trisomy 9 by amniocentesis.
Sherer DM; Wang N; Thompson HO; Peterson JC; Miller ME; Metlay LA; Abramowicz JS
Prenat Diagn; 1992 Jan; 12(1):31-7. PubMed ID: 1557309
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of a fetus with unbalanced translocation (4;13)(p16;q32) with overlapping features of Patau and Wolf-Hirschhorn syndromes.
Tapper JK; Zhang S; Harirah HM; Panova NI; Merryman LS; Hawkins JC; Lockhart LH; Gei AB; Velagaleti GV
Fetal Diagn Ther; 2002; 17(6):347-51. PubMed ID: 12393964
[TBL] [Abstract][Full Text] [Related]
17. Partial deletion of 4p in fetal cells not present in chorionic villi.
Eiben B; Leipoldt M; Schübbe I; Ulbrich R; Hansmann I
Clin Genet; 1988 Jan; 33(1):49-52. PubMed ID: 3277756
[TBL] [Abstract][Full Text] [Related]
18. Partial monosomy 13q and partial trisomy 18p: case report with necropsy findings.
Beneck D; Greco MA; Wolman SR; McMorrow LE; Jansen V; Cason J
J Med Genet; 1986 Jun; 23(3):260-3. PubMed ID: 3723557
[TBL] [Abstract][Full Text] [Related]
19. Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report.
Ahn JM; Koo DH; Kwon KW; Lee YK; Lee YH; Lee HH; Nam KH; Lee KH
J Korean Med Sci; 2003 Feb; 18(1):112-3. PubMed ID: 12589098
[TBL] [Abstract][Full Text] [Related]
20. Prenatal fetal karyotyping and maternal serum alpha-fetoprotein screening.
Gosden C; Buckton K; Fotheringham Z; Brock DJ
Br Med J (Clin Res Ed); 1981 Jan; 282(6260):255-8. PubMed ID: 6161673
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]