128 related articles for article (PubMed ID: 8508672)
1. Confirmation of isochromosome 18p using whole chromosome arm-specific fluorescence in situ hybridization.
Mewar R; Harrison W; Overhauser J
Cytogenet Cell Genet; 1993; 64(1):1-4. PubMed ID: 8508672
[TBL] [Abstract][Full Text] [Related]
2. Identification of iso(18p) marker chromosome by fluorescence in situ hybridization with single-copy DNA probe.
Nakashima H; Hasegawa T; Sakai M; Inaba R; Imamura T
Jpn J Hum Genet; 1995 Jun; 40(2):185-8. PubMed ID: 7662998
[TBL] [Abstract][Full Text] [Related]
3. De novo isochromosome 18p in two patients: cytogenetic diagnosis and confirmation by chromosome painting.
Back E; Toder R; Voiculescu I; Wildberg A; Schempp W
Clin Genet; 1994 Jun; 45(6):301-4. PubMed ID: 7923860
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones.
Popp S; Jauch A; Schindler D; Speicher MR; Lengauer C; Donis-Keller H; Riethman HC; Cremer T
Hum Genet; 1993 Dec; 92(6):527-32. PubMed ID: 8262510
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Tetrasomy 18p in two cases confirmation by in situ hybridization.
Esmer MC; Frias S; Gómez L; Carnevale A
Ann Genet; 1994; 37(3):156-9. PubMed ID: 7847800
[TBL] [Abstract][Full Text] [Related]
8. Chromosomal rearrangements detected by FISH and G-banding.
Hou JW; Wang TR
J Formos Med Assoc; 1996 Sep; 95(9):686-91. PubMed ID: 8918057
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Clinical outcome: a monosomy 18p is better than a tetrasomy 18p.
Wei J; Xie Y; He W; Liu W; Jian W; Chen M; Wang D; Wang X; Sun X
Cytogenet Genome Res; 2014; 144(4):294-8. PubMed ID: 25634515
[TBL] [Abstract][Full Text] [Related]
11. Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.
Horsley SW; Knight SJ; Nixon J; Huson S; Fitchett M; Boone RA; Hilton-Jones D; Flint J; Kearney L
J Med Genet; 1998 Sep; 35(9):722-6. PubMed ID: 9733029
[TBL] [Abstract][Full Text] [Related]
12. Characterization of i(18p) in prenatal diagnosis by fluorescence in situ hybridization.
Yu LC; Williams J; Wang BB; Vooijs M; Weier HU; Sakamoto M; Ying KL
Prenat Diagn; 1993 May; 13(5):355-61. PubMed ID: 8341633
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Marker chromosome identification by micro-FISH.
Engelen JJ; Loots WJ; Motoh PC; Moog U; Hamers GJ; Geraedts JP
Clin Genet; 1996 May; 49(5):242-8. PubMed ID: 8832132
[TBL] [Abstract][Full Text] [Related]
15. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. De novo isochromosome 18p in a female dysmorphic child.
Ramegowda S; Gawde HM; Hyderi A; Savitha MR; Patel ZM; Krishnamurthy B; Ramachandra NB
J Appl Genet; 2006; 47(4):397-401. PubMed ID: 17132906
[TBL] [Abstract][Full Text] [Related]
18. Tetrasomy 18p de novo: parental origin and different mechanisms of formation.
Bugge M; Blennow E; Friedrich U; Petersen MB; Pedeutour F; Tsezou A; Orum A; Hermann S; Lyngbye T; Sarri C; Avramopoulos D; Kitsiou S; Lambert JC; Guzda M; Tommerup N; Brøndum-Nielsen K
Eur J Hum Genet; 1996; 4(3):160-7. PubMed ID: 8840116
[TBL] [Abstract][Full Text] [Related]
19. Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing.
Eggermann T; Engels H; Moskalonek B; Nöthen MM; Müller-Navia J; Schleiermacher E; Schwanitz G; Stengel-Rutkowski S
Hum Genet; 1996 May; 97(5):568-72. PubMed ID: 8655132
[TBL] [Abstract][Full Text] [Related]
20. Incidence of chromosome numerical changes in multiple myeloma: fluorescence in situ hybridization analysis using 15 chromosome-specific probes.
Tabernero D; San Miguel JF; Garcia-Sanz M; Nájera L; García-Isidoro M; Peréz-Simon JA; Gonzalez M; Wiegant J; Raap AK; Orfão A
Am J Pathol; 1996 Jul; 149(1):153-61. PubMed ID: 8686739
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]