131 related articles for article (PubMed ID: 6698562)
1. Premature centromere splitting in a presumptive mild form of Roberts syndrome.
Petrinelli P; Antonelli A; Marcucci L; Dallapiccola B
Hum Genet; 1984; 66(1):96-9. PubMed ID: 6698562
[TBL] [Abstract][Full Text] [Related]
2. The importance of chromosome studies in Roberts syndrome/SC phocomelia and other cohesinopathies.
Gerkes EH; van der Kevie-Kersemaekers AM; Yakin M; Smeets DF; van Ravenswaaij-Arts CM
Eur J Med Genet; 2010; 53(1):40-4. PubMed ID: 19878742
[TBL] [Abstract][Full Text] [Related]
3. Studies of mitotic and centromeric abnormalities in Roberts syndrome: implications for a defect in the mitotic mechanism.
Jabs EW; Tuck-Muller CM; Cusano R; Rattner JB
Chromosoma; 1991 May; 100(4):251-61. PubMed ID: 2055135
[TBL] [Abstract][Full Text] [Related]
4. Cytogenetic findings in Roberts-SC phocomelia syndrome(s).
Tomkins D; Hunter A; Roberts M
Am J Med Genet; 1979; 4(1):17-26. PubMed ID: 495649
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. Premature separation of centromeres in marrow chromosomes from an untreated patient with acute myelogenous leukemia.
Littlefield LG; Joiner EE; Sayer AM
Cancer Genet Cytogenet; 1985 Mar; 16(2):109-16. PubMed ID: 3855690
[TBL] [Abstract][Full Text] [Related]
7. Prenatal ultrasound diagnosis of Roberts syndrome in a family with negative history.
Paladini D; Palmieri S; Lecora M; Perone L; Di Meglio A; D'Armiento M; Cascioli C; Martinelli P
Ultrasound Obstet Gynecol; 1996 Mar; 7(3):208-10. PubMed ID: 8705416
[TBL] [Abstract][Full Text] [Related]
8. Roberts-SC phocomelia syndrome with exencephaly.
Verloes A; Herens C; Van Maldergem L; Retz MC; Dodinval P
Ann Genet; 1989; 32(3):169-70. PubMed ID: 2817778
[TBL] [Abstract][Full Text] [Related]
9. Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.
Turleau C; Cabanis MO; Girault D; Ledeist F; Mettey R; Puissant H; Prieur M; de Grouchy J
Am J Med Genet; 1989 Mar; 32(3):420-4. PubMed ID: 2729362
[TBL] [Abstract][Full Text] [Related]
10. Sister chromatid exchange in the centromere and centromeric area.
Becher R; Sandberg AA
Hum Genet; 1983; 63(4):358-61. PubMed ID: 6862441
[TBL] [Abstract][Full Text] [Related]
11. SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma.
Parry DM; Mulvihill JJ; Tsai SE; Kaiser-Kupfer MI; Cowan JM
Am J Med Genet; 1986 Aug; 24(4):653-72. PubMed ID: 3740099
[TBL] [Abstract][Full Text] [Related]
12. Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes.
Musio A; Mariani T; Montagna C; Zambroni D; Ascoli C; Ried T; Vezzoni P
Gene; 2004 Apr; 331():33-40. PubMed ID: 15094189
[TBL] [Abstract][Full Text] [Related]
13. C-anaphases in lymphocyte cultures versus premature centromere division syndromes.
Chamla Y
Hum Genet; 1988 Feb; 78(2):111-4. PubMed ID: 3276615
[TBL] [Abstract][Full Text] [Related]
14. Chromatid repulsion associated with Roberts/SC phocomelia syndrome is reduced in malignant cells and not expressed in interspecies somatic-cell hybrids.
Krassikoff NE; Cowan JM; Parry DM; Francke U
Am J Hum Genet; 1986 Nov; 39(5):618-30. PubMed ID: 3788975
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Centromere spreading and out-of-phase chromatid separation in Burkitt's lymphoma and nasopharyngeal carcinoma.
Zhang SH
Cancer Genet Cytogenet; 1986 Nov; 23(3):211-7. PubMed ID: 3768847
[TBL] [Abstract][Full Text] [Related]
17. Rhabdomyosarcoma in Roberts syndrome.
Wenger SL; Blatt J; Steele MW; Lloyd DA; Bellinger M; Phebus CK; Horn M; Jaffe R
Cancer Genet Cytogenet; 1988 Apr; 31(2):285-9. PubMed ID: 3349442
[TBL] [Abstract][Full Text] [Related]
18. Deletion of the centromere as a mechanism for achieving stability of a dicentric chromosome.
Vianna-Morgante AM; Rosenberg C
Cytogenet Cell Genet; 1986; 42(3):119-22. PubMed ID: 3731880
[TBL] [Abstract][Full Text] [Related]
19. A mild form of Roberts/SC phocomelia syndrome with asymmetrical reduction of the upper limbs.
Concolino D; Sperlì D; Cinti R; Strisciuglio P; Andria G
Clin Genet; 1996 May; 49(5):274-6. PubMed ID: 8832138
[TBL] [Abstract][Full Text] [Related]
20. Premature centromere division (PCD): a dominantly inherited cytogenetic anomaly.
Madan K; Lindhout D; Palan A
Hum Genet; 1987 Oct; 77(2):193-6. PubMed ID: 3653892
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
