368 related articles for article (PubMed ID: 1928105)
1. De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.
Warburton D
Am J Hum Genet; 1991 Nov; 49(5):995-1013. PubMed ID: 1928105
[TBL] [Abstract][Full Text] [Related]
2. Prenatally diagnosed balanced chromosome rearrangements: eight years' experience.
Peng HH; Chao AS; Wang TH; Chang YL; Chang SD
J Reprod Med; 2006 Sep; 51(9):699-703. PubMed ID: 17039698
[TBL] [Abstract][Full Text] [Related]
3. De novo balanced chromosome rearrangements in prenatal diagnosis.
Giardino D; Corti C; Ballarati L; Colombo D; Sala E; Villa N; Piombo G; Pierluigi M; Faravelli F; Guerneri S; Coviello D; Lalatta F; Cavallari U; Bellotti D; Barlati S; Croci G; Franchi F; Savin E; Nocera G; Amico FP; Granata P; Casalone R; Nutini L; Lisi E; Torricelli F; Giussani U; Facchinetti B; Guanti G; Di Giacomo M; Susca FP; Pecile V; Romitti L; Cardarelli L; Racalbuto E; Police MA; Chiodo F; Rodeschini O; Falcone P; Donti E; Grimoldi MG; Martinoli E; Stioui S; Caufin D; Lauricella SA; Tanzariello SA; Voglino G; Lenzini E; Besozzi M; Larizza L; Dalprà L
Prenat Diagn; 2009 Mar; 29(3):257-65. PubMed ID: 19248039
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of a fetus with two balanced de novo chromosome rearrangements.
Cotter PD; Caggana M; Willner JP; Babu A; Desnick RJ
Am J Med Genet; 1996 Dec; 66(2):197-9. PubMed ID: 8958330
[TBL] [Abstract][Full Text] [Related]
5. Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis.
Warburton D
Prenat Diagn; 1984; 4 Spec No():69-80. PubMed ID: 6463034
[TBL] [Abstract][Full Text] [Related]
6. De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.
Bonthron DT; Smith SJ; Fantes J; Gosden CM
Am J Hum Genet; 1993 Sep; 53(3):629-37. PubMed ID: 8352273
[TBL] [Abstract][Full Text] [Related]
7. De novo double reciprocal translocations in addition to partial monosomy at another chromosome: A very rare case.
Simioni M; Steiner CE; Gil-da-Silva-Lopes VL
Gene; 2015 Nov; 573(1):166-70. PubMed ID: 26318482
[TBL] [Abstract][Full Text] [Related]
8. Robertsonian translocation and an extra microchromosome: independent origin identified by in situ hybridization.
Heppell-Parton AC; Waters JJ
Clin Genet; 1991 Feb; 39(2):93-6. PubMed ID: 2015699
[TBL] [Abstract][Full Text] [Related]
9. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: two new cases and review of the literature.
Ruiz C; Grubs RE; Jewett T; Cox-Jones K; Abruzzese E; Pettenati MJ; Rao PN
Am J Med Genet; 1996 Aug; 64(3):478-84. PubMed ID: 8862625
[TBL] [Abstract][Full Text] [Related]
10. The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age.
Van Dyke DL; Weiss L; Roberson JR; Babu VR
Am J Hum Genet; 1983 Mar; 35(2):301-8. PubMed ID: 6837576
[TBL] [Abstract][Full Text] [Related]
11. Frequencies of fetal chromosomal abnormalities at prenatal diagnosis: 10 years experiences in a single institution.
Park SY; Kim JW; Kim YM; Kim JM; Lee MH; Lee BY; Han JY; Kim MY; Yang JH; Ryu HM
J Korean Med Sci; 2001 Jun; 16(3):290-3. PubMed ID: 11410688
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.
Daniel A; Hook EB; Wulf G
Am J Med Genet; 1989 May; 33(1):14-53. PubMed ID: 2750783
[TBL] [Abstract][Full Text] [Related]
14. [Incidence and significance of chromosomal translocations in prenatal diagnosis].
Wolff F; Schaefer R; Bolte A
Geburtshilfe Frauenheilkd; 1986 Jun; 46(6):359-62. PubMed ID: 3744005
[TBL] [Abstract][Full Text] [Related]
15. Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes.
Berend SA; Horwitz J; McCaskill C; Shaffer LG
Am J Hum Genet; 2000 Jun; 66(6):1787-93. PubMed ID: 10775524
[TBL] [Abstract][Full Text] [Related]
16. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
Hsu LY; Yu MT; Richkind KE; Van Dyke DL; Crandall BF; Saxe DF; Khodr GS; Mennuti M; Stetten G; Miller WA; Priest JH
Prenat Diagn; 1996 Jan; 16(1):1-28. PubMed ID: 8821848
[TBL] [Abstract][Full Text] [Related]
17. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
Chen CP; Chern SR; Wu PC; Tsai FJ; Lee CC; Town DD; Chen WL; Chen LF; Lee MS; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2009 Dec; 48(4):389-99. PubMed ID: 20045761
[TBL] [Abstract][Full Text] [Related]
18. Balanced chromosome translocations and abnormal phenotypes. A report of 5 cases.
van Heerden KM; de Jong G; Fox MF; Kotzé GM; Brusnický J; Dietzsch E; Grobbelaar JJ; Retief AE
S Afr Med J; 1986 Jun; 69(13):825-7. PubMed ID: 3715666
[TBL] [Abstract][Full Text] [Related]
19. A case of mosaicism involving an unstable 13/14 Robertsonian translocation.
Wells S; Gregson N; Porter RJ
Prenat Diagn; 1991 Nov; 11(11):875-80. PubMed ID: 1754558
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of a de novo complex chromosomal rearrangement involving four chromosomes.
Kim HJ; Perle MA; Bogosian V; Greco A
Prenat Diagn; 1986; 6(3):211-6. PubMed ID: 3725740
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
