266 related articles for article (PubMed ID: 8357009)
1. Isochromosome 18p in a mother and her child.
Abeliovich D; Dagan J; Levy A; Steinberg A; Zlotogora J
Am J Med Genet; 1993 Jun; 46(4):392-3. PubMed ID: 8357009
[TBL] [Abstract][Full Text] [Related]
2. Tetrasomy 18p in a child with trisomy 18 phenotype.
Singer TS; Kohn G; Yatziv S
Am J Med Genet; 1990 Jun; 36(2):144-7. PubMed ID: 2368801
[TBL] [Abstract][Full Text] [Related]
3. Tetrasomy 18p: a distinctive syndrome.
Rivera H; Möller M; Hernández A; Enríquez-Guerra MA; Arreola R; Cantú JM
Ann Genet; 1984; 27(3):187-9. PubMed ID: 6334486
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
Habecker-Green JG; Naeem R; Gold H; O'Grady JP; Kanaan C; Bayer-Zwirello L; Murray MS; Cohn GM
J Perinatol; 1998; 18(5):395-8. PubMed ID: 9766419
[TBL] [Abstract][Full Text] [Related]
5. Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomes.
Park VM; Gustashaw KM; Bilenker RM; Golden WL
Am J Med Genet; 1991 Nov; 41(2):180-3. PubMed ID: 1785630
[TBL] [Abstract][Full Text] [Related]
6. Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.
Urioste M; Visedo G; Sanchís A; Sentís C; Villa A; Ludeña P; Hortigüela JL; Martínez-Frías ML; Fernández-Piqueras J
Am J Med Genet; 1994 Jan; 49(1):77-82. PubMed ID: 8172255
[TBL] [Abstract][Full Text] [Related]
7. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
Shapiro SD; Hansen KL; Littlefield CA
Am J Med Genet; 1985 Feb; 20(2):271-6. PubMed ID: 3976720
[TBL] [Abstract][Full Text] [Related]
8. A patient with hypopituitarism and isochromosome 18q mosaicism.
Turan S; Saka N; Guney I; Bereket A
Horm Res; 2005; 64(6):261-5. PubMed ID: 16272819
[TBL] [Abstract][Full Text] [Related]
9. [Tetrasomy 18p: report of a case].
Borrego López S; Nieto Barrera M; Antiñolo Gil G; Sánchez García J; de la Rosa Oliver A
An Esp Pediatr; 1988 Jul; 29(1):80-2. PubMed ID: 3056147
[No Abstract] [Full Text] [Related]
10. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
11. [Rare case of mosaicism for chromosome 18, karyotype: 46, XX, del(18) (p11)/46, XX, i(18q)].
Badalian LO; Mutovin GR; Malygina NA; Petrukhin AS
Genetika; 1983 Nov; 19(11):1912-5. PubMed ID: 6686175
[TBL] [Abstract][Full Text] [Related]
12. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
[TBL] [Abstract][Full Text] [Related]
13. [Tetrasomy of the short arm of human chromosome 18: cytogenetics and phenotypic disorders].
Kuleshov NP; Zaletaev DV; Levina LIa; Dement'eva GM; Arbuzov SP
Tsitol Genet; 1985; 19(6):452-6. PubMed ID: 4089954
[TBL] [Abstract][Full Text] [Related]
14. Mosaic tetrasomy 12p: four new cases, and confirmation of the chromosomal origin of the supernumerary chromosome in one of the original Pallister-Mosaic syndrome cases.
Warburton D; Anyane-Yeboa K; Francke U
Am J Med Genet; 1987 Jun; 27(2):275-83. PubMed ID: 3605213
[TBL] [Abstract][Full Text] [Related]
15. Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters.
Boyle J; Sangha K; Dill F; Robinson WP; Yong SL
Am J Med Genet; 2001 Jun; 101(1):65-9. PubMed ID: 11343341
[TBL] [Abstract][Full Text] [Related]
16. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
[TBL] [Abstract][Full Text] [Related]
17. The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.
Callen DF; Freemantle CJ; Ringenbergs ML; Baker E; Eyre HJ; Romain D; Haan EA
Am J Hum Genet; 1990 Sep; 47(3):493-8. PubMed ID: 2393023
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Tetrasomy 9p: tissue-limited idic(9p) in a child with mild manifestations and a normal CVS result. Report and review.
Grass FS; Parke JC; Kirkman HN; Christensen V; Roddey OF; Wade RV; Knutson C; Spence JE
Am J Med Genet; 1993 Nov; 47(6):812-6. PubMed ID: 7506483
[TBL] [Abstract][Full Text] [Related]
20. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F
J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]