90 related articles for article (PubMed ID: 2389794)
1. Origin of 46,XY/46,XY,r(19) mosaicism.
Yung JF; Sobel DB; Hoo JJ
Am J Med Genet; 1990 Aug; 36(4):391-3. PubMed ID: 2389794
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Monosomy 8 rescue gave cells with a normal karyotype in a mildly affected man with 46,XY,r(8) mosaicism.
Gradek GA; Kvistad PH; Houge G
Eur J Med Genet; 2006; 49(4):292-7. PubMed ID: 16829350
[TBL] [Abstract][Full Text] [Related]
5. Ring chromosome 4 mosaicism and Potter sequence.
Fryns JP; Kleczkowska A; Jaeken J; Van den Berghe H
Ann Genet; 1988; 31(2):120-2. PubMed ID: 3261147
[TBL] [Abstract][Full Text] [Related]
6. Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.
Baumer A; Giovannucci Uzielli ML; Guarducci S; Lapi E; Röthlisberger B; Schinzel A
Am J Med Genet; 2002 Nov; 113(1):101-4. PubMed ID: 12400074
[TBL] [Abstract][Full Text] [Related]
7. Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype.
Wieczorek D; Prott EC; Robinson WP; Passarge E; Gillessen-Kaesbach G
Prenat Diagn; 2003 Feb; 23(2):128-33. PubMed ID: 12575019
[TBL] [Abstract][Full Text] [Related]
8. [Ring chromosomes in mosaicism 46, XY, Cr-46, XY].
Ferrier S; Freund M; Grétillat A
Arch Genet (Zur); 1973; 46(1):1-14. PubMed ID: 4731928
[No Abstract] [Full Text] [Related]
9. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G
J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374
[TBL] [Abstract][Full Text] [Related]
10. A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome.
Roberts E; Dunlop J; Davis GS; Churchill D; Davison EV
Prenat Diagn; 2003 Jul; 23(7):564-5. PubMed ID: 12868084
[TBL] [Abstract][Full Text] [Related]
11. Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)].
Sijmons RH; Leegte B; van Lingen RA; de Pater JM; van der Veen AY; del Canho H; Bos C; ten Kate LP; Breed AS
Am J Med Genet; 1993 Sep; 47(4):559-62. PubMed ID: 7504882
[TBL] [Abstract][Full Text] [Related]
12. [Terminal partial mosaic monosomy of the short arm of chromosome 3, in discordant monozygotic twins, 46,XY/46,XY, del (3) (p25)].
Bueno I; Olivares JL; Olmedillas MJ; Abad M; Bueno M
An Esp Pediatr; 1987 Mar; 26(3):187-90. PubMed ID: 3579058
[TBL] [Abstract][Full Text] [Related]
13. Hypomelanosis of ito with trisomy 13 mosaicism [46, XY, der (13;13) (q10;q10), +13/46,xy].
Yakinci C; Kutlu NO; Alp MN; Senol M; Durmaz Y; Budak T
Turk J Pediatr; 2002; 44(2):152-5. PubMed ID: 12026206
[TBL] [Abstract][Full Text] [Related]
14. A case of ring (9)/del(9p) mosaicism associated with gastroesophageal reflux.
Leung AK; Rudd NL
Am J Med Genet; 1988 Jan; 29(1):43-8. PubMed ID: 3344775
[TBL] [Abstract][Full Text] [Related]
15. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
[TBL] [Abstract][Full Text] [Related]
16. Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex.
Costa T; Lambert M; Teshima I; Ray PN; Richer CL; Dallaire L
Am J Med Genet; 1998 Jan; 75(1):40-4. PubMed ID: 9450855
[TBL] [Abstract][Full Text] [Related]
17. Lens dislocation and optic nerve hypoplasia in ring chromosome 21 mosaicism.
Meire FM; Fryns JP
Ann Genet; 1994; 37(3):150-2. PubMed ID: 7847798
[TBL] [Abstract][Full Text] [Related]
18. Ring chromosome 6: case report and review.
Nishi Y; Yoshimura O; Ohama K; Usui T
Am J Med Genet; 1982 May; 12(1):109-14. PubMed ID: 7091194
[TBL] [Abstract][Full Text] [Related]
19. Another patient with a deletion 14q11.2q13.
Govaerts L; Toorman J; Blij-Philipsen MV; Smeets D
Ann Genet; 1996; 39(4):197-200. PubMed ID: 9037346
[TBL] [Abstract][Full Text] [Related]
20. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
