113 related articles for article (PubMed ID: 2369070)
1. Ring chromosome 21 transmitted from mother to daughter: its stability in a lymphoblastoid cell line.
Ikeuchi T; Yamamoto K; Qiao F; Hayakawa K; Migita T; Nishikawa Y
Ann Genet; 1990; 33(1):32-5. PubMed ID: 2369070
[TBL] [Abstract][Full Text] [Related]
2. Ring chromosome 16: a new case.
Vianello MG; Cottafava F; Bartoli D; Franzone G; Casazzava R; Gastaldi R
Ann Genet; 1990; 33(1):36-9. PubMed ID: 2195979
[TBL] [Abstract][Full Text] [Related]
3. Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son.
Fryns JP; Kleczkowska A; Smeets E; Van Den Berghe H
Ann Genet; 1992; 35(2):121-3. PubMed ID: 1524410
[TBL] [Abstract][Full Text] [Related]
4. Familial ring (19) chromosome mosaicism: case report and review.
Flejter WL; Finlinson D; Root S; Nguyen W; Brothman AR; Viskochil D
Am J Med Genet; 1996 Dec; 66(3):276-80. PubMed ID: 8985487
[TBL] [Abstract][Full Text] [Related]
5. Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype.
Jenderny J; Caliebe A; Beyer C; Grote W
J Med Genet; 1993 Nov; 30(11):964-5. PubMed ID: 8301656
[TBL] [Abstract][Full Text] [Related]
6. [Ring chromosome 4 in twins].
Giuffrè L; Cammarata M; Corsello G; Benigno V; Graziano L; Roccella F; Balsamo V
Pediatr Med Chir; 1987; 9(3):349-50. PubMed ID: 3671134
[TBL] [Abstract][Full Text] [Related]
7. Identification of marker chromosomes in thirteen patients using FISH probing.
Daniel A; Malafiej P; Preece K; Chia N; Nelson J; Smith M
Am J Med Genet; 1994 Oct; 53(1):8-18. PubMed ID: 7802042
[TBL] [Abstract][Full Text] [Related]
8. Balanced complex rearrangement involving chromosomes 8, 9, and 12 in a normal mother, derivative chromosome 9 with recombinant chromosome 12 in her daughter with minor anomalies.
Masuno M; Asano J; Yasuda K; Kondo T; Orii T
Am J Med Genet; 1993 Jan; 45(1):65-7. PubMed ID: 8418663
[TBL] [Abstract][Full Text] [Related]
9. Ring chromosome 2 in a child with growth failure and few congenital abnormalities.
Vigfusson NV; Kapstafer KJ; Lloyd MA
Am J Med Genet; 1980; 7(3):383-9. PubMed ID: 7468662
[TBL] [Abstract][Full Text] [Related]
10. A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.
Gibson LH; McGrath J; Yang-Feng TL
Am J Med Genet; 1997 Feb; 68(4):417-20. PubMed ID: 9021014
[TBL] [Abstract][Full Text] [Related]
11. Ring chromosome 22 and autism: report and review.
MacLean JE; Teshima IE; Szatmari P; Nowaczyk MJ
Am J Med Genet; 2000 Feb; 90(5):382-5. PubMed ID: 10706359
[TBL] [Abstract][Full Text] [Related]
12. [Ring chromosome 13 (type I) 45,XY,-13/46, XY,r(13)(p11:q34)].
Díaz-Cardama Sousa I; Mora Gandarillas I; Vázquez Rodríguez M; Viso Lorenzo A; Alonso Villa MJ; Fernández Toral J
An Esp Pediatr; 1990 Jun; 32(6):556-8. PubMed ID: 2221637
[No Abstract] [Full Text] [Related]
13. Application of fluorescence in situ hybridization to the identification of different marker chromosomes.
Verschraegen-Spae MR; Quack B; Rousseaux S; Pison H; Messiaen L; De Paepe A; Lespinasse J
Ann Genet; 1998; 41(1):5-10. PubMed ID: 9599644
[TBL] [Abstract][Full Text] [Related]
14. Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism.
Nowaczyk MJ; Ramsay JA; Mohide P; Tomkins DJ
Am J Med Genet; 1998 May; 77(4):306-9. PubMed ID: 9600741
[TBL] [Abstract][Full Text] [Related]
15. Dystonia in a patient with ring chromosome 21.
Hou CE; Schlaggar BL; Racette BA
Mov Disord; 2003 Dec; 18(12):1547-9. PubMed ID: 14673898
[TBL] [Abstract][Full Text] [Related]
16. [Van der Woude syndrome in combination with ring chromosome 18].
Kalker U; Gabriel M; Jacobi G
Monatsschr Kinderheilkd; 1988 Feb; 136(2):95-8. PubMed ID: 3367915
[TBL] [Abstract][Full Text] [Related]
17. Familial transmission of a ring chromosome 21.
Hertz JM
Clin Genet; 1987 Jul; 32(1):35-9. PubMed ID: 2887318
[TBL] [Abstract][Full Text] [Related]
18. [Ring chromosome 9].
Kontiokari T; Borgström GH; Ritanen-Mohammed UM
Duodecim; 1995; 111(5):439-41. PubMed ID: 8674446
[No Abstract] [Full Text] [Related]
19. Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patient.
Juyal RC; Finucane B; Shaffer LG; Lupski JR; Greenberg F; Scott CI; Baldini A; Patel PI
Am J Med Genet; 1995 Nov; 59(3):406-7. PubMed ID: 8599375
[No Abstract] [Full Text] [Related]
20. Ring chromosome 21. Observation in a female infant.
Carlo Stella N; Barberi I; Corrado F; Triolo O
Ann Genet; 1984; 27(4):249-51. PubMed ID: 6335374
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]