105 related articles for article (PubMed ID: 3499846)
1. Incidental finding of double minutes (DM), single minutes (SM), homogenously staining regions (HSR), premature chromosome condensation (PCC), and premature centromere division (PCD)?
Bühler EM; Fessler R; Beutler C; Gargano G
Ann Genet; 1987; 30(2):75-9. PubMed ID: 3499846
[TBL] [Abstract][Full Text] [Related]
2. Premature centromere division in three unrelated families.
Keser I; Lüleci G; Gündüz G
Ann Genet; 1996; 39(2):87-90. PubMed ID: 8766139
[TBL] [Abstract][Full Text] [Related]
3. Premature centromere division: a possible manifestation of chromosome instability.
Méhes K; Bühler EM
Am J Med Genet; 1995 Mar; 56(1):76-9. PubMed ID: 7747791
[TBL] [Abstract][Full Text] [Related]
4. Familial chromosomal aberrations. I.
Zellweger H
Ann Paediatr; 1966; 206(5):317-32. PubMed ID: 4225154
[No Abstract] [Full Text] [Related]
5. Autosomal mosaicism in amniotic fluid cells from a twin pregnancy.
Greenberg F; Elsas NT; Reidy JA; Chen AT; Stone LB
Am J Med Genet; 1982 Jan; 11(1):109-12. PubMed ID: 7064998
[TBL] [Abstract][Full Text] [Related]
6. [The nature of 3 cytogenetic phenomena--delayed spiralization of regions of the metaphase chromosomes, delayed disruption of the telomeric links of chromosomes and the premature division of X-chromosome centromeres].
Stobetskiĭ VI
Tsitologiia; 1988 Oct; 30(10):1270-2. PubMed ID: 3072745
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of Roberts syndrome: two new cases.
Benzacken B; Savary JB; Manouvrier S; Bucourt M; Gonzales J
Prenat Diagn; 1996 Feb; 16(2):125-30. PubMed ID: 8650122
[TBL] [Abstract][Full Text] [Related]
8. Class II neocentromeres: a putative common neocentromere site in band 4q21.2.
Warburton PC; Barwell J; Splitt M; Maxwell D; Bint S; Ogilvie CM
Eur J Hum Genet; 2003 Oct; 11(10):749-53. PubMed ID: 14512964
[TBL] [Abstract][Full Text] [Related]
9. Twins with nonconcordant sexual aneuploidy.
Garcia-Sagredo JM; Merello-Godino C; San Roman C
J Med Genet; 1977 Jun; 14(3):226-8. PubMed ID: 560486
[TBL] [Abstract][Full Text] [Related]
10. [Roberts' syndrome. Review of the literature and presentation of 2 clinical cases].
Colombo B; Bottelli A; Maserati E
Pediatr Med Chir; 1986; 8(3):411-3. PubMed ID: 3786205
[TBL] [Abstract][Full Text] [Related]
11. Cell cycle and centromere FISH studies in premature centromere division.
Corona-Rivera A; Salamanca-Gomez F; Bobadilla-Morales L; Corona-Rivera JR; Palomino-Cueva C; Garcia-Cobian TA; Corona-Rivera E
BMC Med Genet; 2005 Sep; 6():33. PubMed ID: 16174301
[TBL] [Abstract][Full Text] [Related]
12. Double trisomy (48,XXY,+21) in monozygotic twins: case report and review of the literature.
Iliopoulos D; Poultsides G; Peristeri V; Kouri G; Andreou A; Voyiatzis N
Ann Genet; 2004; 47(1):95-8. PubMed ID: 15050879
[TBL] [Abstract][Full Text] [Related]
13. Centromere separation sequence in aged women and men.
Bajnóczky K
Acta Biol Hung; 1985; 36(3-4):313-8. PubMed ID: 2951954
[TBL] [Abstract][Full Text] [Related]
14. Premature centromere division dominantly inherited in a subfertile family.
Gabarrón J; Jimenez A; Glover G
Cytogenet Cell Genet; 1986; 43(1-2):69-71. PubMed ID: 3780318
[TBL] [Abstract][Full Text] [Related]
15. [Genetic determination of the activity of nucleolar-organizing regions of human chromosomes].
Egolina NA; Davudov AZ; Beniush VA; Zakharov AF
Biull Eksp Biol Med; 1981 Mar; 91(3):350-3. PubMed ID: 7195749
[TBL] [Abstract][Full Text] [Related]
16. Non-random centromere division: analysis of G-banded human chromosomes.
Méhes K; Bajnóczky K
Acta Biol Acad Sci Hung; 1981; 32(1):55-9. PubMed ID: 7282209
[TBL] [Abstract][Full Text] [Related]
17. Cytogenetic observations on two ovarian carcinomas with double minutes, one with a 6q- marker chromosome.
Bullerdiek J; Bartnitzke S; Kahrs E; Schloot W
Cytobios; 1985; 42(165):15-24. PubMed ID: 3858061
[TBL] [Abstract][Full Text] [Related]
18. [Crying cat disease associated with complex chromosome rearrangement in a dizygotic twin].
Taillemite JL; Baheux-Morlier G; Cathelineau L; Roux C
Ann Genet; 1973 Jun; 16(2):127-30. PubMed ID: 4541905
[No Abstract] [Full Text] [Related]
19. Prenatal diagnosis. Results of cytogenetic analysis of amniotic fluid cell cultures.
Mulcahy MT; Jenkyn J
Med J Aust; 1973 May; 1(20):979-82. PubMed ID: 4268556
[No Abstract] [Full Text] [Related]
20. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.
Peschka B; Leygraaf J; Hansmann D; Hansmann M; Schröck E; Ried T; Engels H; Schwanitz G; Schubert R
Prenat Diagn; 1999 Dec; 19(12):1143-9. PubMed ID: 10590433
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]