490 related articles for article (PubMed ID: 16470734)
1. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
[TBL] [Abstract][Full Text] [Related]
2. Complex chromosome rearrangements and congenital anomalies.
Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
[TBL] [Abstract][Full Text] [Related]
3. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
Legare JM; Sekhon GS; Laxova R
Am J Med Genet; 1994 Nov; 53(3):216-21. PubMed ID: 7856655
[TBL] [Abstract][Full Text] [Related]
4. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
Batista DA; Pai GS; Stetten G
Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
[TBL] [Abstract][Full Text] [Related]
5. Two chromosome aberrations in the child of a woman with systemic lupus erythematosus treated with azathioprine and prednisone.
Ostrer H; Stamberg J; Perinchief P
Am J Med Genet; 1984 Mar; 17(3):627-32. PubMed ID: 6711614
[TBL] [Abstract][Full Text] [Related]
6. Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25).
Makita Y; Masuno M; Imaizumi K; Yamashita S; Ohba S; Ito D; Kuroki Y
Am J Med Genet; 1995 May; 57(1):19-21. PubMed ID: 7645592
[TBL] [Abstract][Full Text] [Related]
7. Ultrasound-adjusted risk and spectrum of fetal chromosomal abnormality in women with elevated maternal serum alpha-fetoprotein.
Megerian G; Godmilow L; Donnenfeld AE
Obstet Gynecol; 1995 Jun; 85(6):952-6. PubMed ID: 7539525
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of and midtrimester pathology with karyotype 46,XY,del(4)(q22q26). A case report.
Koppitch FC; Ramahi A; Quereshi F; Budev H; Perrin E; Evans MI
J Reprod Med; 1990 Feb; 35(2):182-6. PubMed ID: 2304042
[TBL] [Abstract][Full Text] [Related]
9. Prenatal detection of cyclopia associated with interstitial deletion of 2p.
Grundy HO; Niemeyer P; Rupani MK; Ward VF; Wassman ER
Am J Med Genet; 1989 Oct; 34(2):268-70. PubMed ID: 2817010
[TBL] [Abstract][Full Text] [Related]
10. Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysis.
Martin AO; Northrup H; Ledbetter DH; Trask B; van den Engh G; Le Beau MM; Beaudet AL; Gray JW; Sekhon G; Krassikoff N
Am J Med Genet; 1988 Nov; 31(3):643-54. PubMed ID: 3228143
[TBL] [Abstract][Full Text] [Related]
11. Balanced complex chromosomal rearrangements with more than four breakpoints: report of a new case.
Till M; Devillard F; Crost P; Bachy M; Prieur F; Berthéas MF
Am J Med Genet; 1991 Sep; 40(3):370-3. PubMed ID: 1951445
[TBL] [Abstract][Full Text] [Related]
12. Trisomy/partial monosomy 13 mosaicism associated with relatively mild clinical malformation.
Duckett DP; Porter HJ; Young ID
Ann Genet; 1992; 35(2):113-6. PubMed ID: 1524408
[TBL] [Abstract][Full Text] [Related]
13. Balanced nonacrocentric whole-arm reciprocal translocations: a de novo case and literature review.
Farrell SA; Fan YS
Am J Med Genet; 1995 Feb; 55(4):423-6. PubMed ID: 7762581
[TBL] [Abstract][Full Text] [Related]
14. Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literature.
Münke M; Emanuel BS; Zackai EH
Am J Med Genet; 1988 Aug; 30(4):929-38. PubMed ID: 3055987
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection.
Benn PA; Hsu LY; Verma RS; Alonso ML; Reich E; Wishnick M
Obstet Gynecol; 1987 Sep; 70(3 Pt 2):449-52. PubMed ID: 3627600
[TBL] [Abstract][Full Text] [Related]
16. Translocation/duplication of 9p onto a duplicated 4q.
Rivera H; Figuera LE; Vasquez AI
Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
[TBL] [Abstract][Full Text] [Related]
17. Midtrimester diagnosis and anomalies in the dup(22q) syndrome: correlation of aneuploidy with low maternal serum alpha-fetoprotein and oligohydramnios.
Johnson MP; Greb A; Goyert G; Drugan A; Qureshi F; Sacks AJ; Evans MI
Am J Med Genet; 1990 May; 36(1):94-6. PubMed ID: 1692182
[TBL] [Abstract][Full Text] [Related]
18. Small marker chromosome mosaicism confirmed in two cases ascertained prenatally.
Kohn G; Shaham M; Ornoy A; Beyth Y; Cohen MM
Am J Med Genet; 1978; 2(2):167-73. PubMed ID: 299455
[TBL] [Abstract][Full Text] [Related]
19. Inherited translocation t(4;5) discovered on prenatal diagnosis.
Sun NH; Wang FY; Li JX; Zhou XT; Tang HS
Am J Med Genet; 1981; 8(3):299-303. PubMed ID: 7234900
[TBL] [Abstract][Full Text] [Related]
20. Report of two cases of distal deletion of the long arm of chromosome 6.
Stevens CA; Fineman RM; Breg WR; Silken AB
Am J Med Genet; 1988 Apr; 29(4):807-14. PubMed ID: 3400725
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
