298 related articles for article (PubMed ID: 21199750)
21. Prenatal diagnosis and prenatal imaging features of fetal monosomy 1p36.
Lissauer D; Larkins SA; Sharif S; MacPherson L; Rhodes C; Kilby MD
Prenat Diagn; 2007 Sep; 27(9):874-8. PubMed ID: 17582615
[TBL] [Abstract][Full Text] [Related]
22. Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation.
Lennon PA; Cooper ML; Curtis MA; Lim C; Ou Z; Patel A; Cheung SW; Bacino CA
Am J Med Genet A; 2006 Jun; 140(11):1156-63. PubMed ID: 16688748
[TBL] [Abstract][Full Text] [Related]
23. Trisomy 1q42-qter associated with monosomy 6q27-qter: a case report.
Tartaglia E; Mastrantonio P; Costa D; Giugliano B; Porcellini A; Costagliola C
Eur J Ophthalmol; 2011; 21(3):315-9. PubMed ID: 20954143
[TBL] [Abstract][Full Text] [Related]
24. Prenatal diagnosis of partial monosomy 13q associated with occipital encephalocoele in a fetus.
Chen CP; Liu FF; Jan SW; Wang KG; Lan CC
Prenat Diagn; 1996 Jul; 16(7):664-6. PubMed ID: 8843478
[TBL] [Abstract][Full Text] [Related]
25. Prenatal diagnosis and molecular cytogenetic analysis of a de novo isodicentric chromosome 18.
Zhang Y; Dai Y; Ren J; Wang L
Ann Saudi Med; 2010; 30(6):489-92. PubMed ID: 20864786
[TBL] [Abstract][Full Text] [Related]
26. Unbalanced translocation 6p/16q (partial monosomy 6p and trisomy 16q): prenatal diagnosis and cytogenetics.
Puhl AG; Zelazny J; Galetzka D; Skala C; Frey-Mahn G; Wellek B; Koelbl H
Eur J Obstet Gynecol Reprod Biol; 2010 Jun; 150(2):119-25. PubMed ID: 20211513
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Prenatal diagnosis of a large de novo terminal deletion of chromosome 11q.
Boehm D; Laccone F; Burfeind P; Herold S; Schubert C; Zoll B; Männer J; Pauer HU; Bartels I
Prenat Diagn; 2006 Mar; 26(3):286-90. PubMed ID: 16506277
[TBL] [Abstract][Full Text] [Related]
29. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
Chen CP; Lin SP; Chern SR; Shih SL; Lee CC; Wang W; Liao YW
Prenat Diagn; 2003 Jun; 23(6):504-8. PubMed ID: 12813767
[TBL] [Abstract][Full Text] [Related]
30. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
McGhee EM; Qu Y; Wohlferd MM; Goldberg JD; Norton ME; Cotter PD
Clin Genet; 2001 Apr; 59(4):274-8. PubMed ID: 11298684
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Prenatal diagnosis of a recombinant chromosome 7 resulting in trisomy 7q11.22 --> qter.
Tchirikov M; Merinsky A; Strohner M; Bonin M; Beyer V; Haaf T; Bartsch O
Am J Med Genet A; 2010 Mar; 152A(3):721-5. PubMed ID: 20186810
[TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.
Chen CP; Liu FF; Jan SW; Lin SP; Lan CC
Prenat Diagn; 1996 Mar; 16(3):270-5. PubMed ID: 8710784
[TBL] [Abstract][Full Text] [Related]
34. Del(18p) syndrome with increased nuchal translucency in prenatal diagnosis.
Kim YM; Cho EH; Kim JM; Lee MH; Park SY; Ryu HM
Prenat Diagn; 2004 Mar; 24(3):161-4. PubMed ID: 15057945
[TBL] [Abstract][Full Text] [Related]
35. Prenatal diagnosis of de novo trisomy 1(q21-qter)der(Y)t(Y;1) in a malformed live born.
Fernández-Novoa MC; Vargas MT; Granell MR; Carreto P
Prenat Diagn; 2004 Jun; 24(6):414-7. PubMed ID: 15229838
[TBL] [Abstract][Full Text] [Related]
36. Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion.
Chen CP; Chang TY; Shih JC; Lin SP; Lin CJ; Wang W; Lee CC; Town DD; Pan CW; Tzen CY
Prenat Diagn; 2002 Dec; 22(12):1063-6. PubMed ID: 12454959
[TBL] [Abstract][Full Text] [Related]
37. Prenatal diagnosis of mosaic distal 5p deletion and review of the literature.
Chen CP; Lee CC; Chang TY; Town DD; Wang W
Prenat Diagn; 2004 Jan; 24(1):50-7. PubMed ID: 14755410
[TBL] [Abstract][Full Text] [Related]
38. Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature.
Malan V; Martinovic J; Sanlaville D; Caillat S; Waill MC; Ganne ML; Tantau J; Attie-Bitach T; Vekemans M; Morichon-Delvallez N
Prenat Diagn; 2006 Mar; 26(3):231-8. PubMed ID: 16450350
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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]
[Previous] [Next] [New Search]