279 related articles for article (PubMed ID: 9856565)
1. Identification of an unusual marker chromosome by spectral karyotyping.
Huang B; Ning Y; Lamb AN; Sandlin CJ; Jamehdor M; Ried T; Bartley J
Am J Med Genet; 1998 Dec; 80(4):368-72. PubMed ID: 9856565
[TBL] [Abstract][Full Text] [Related]
2. Tetrasomy 15q25-->qter: cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome.
Rowe AG; Abrams L; Qu Y; Chen E; Cotter PD
Am J Med Genet; 2000 Aug; 93(5):393-8. PubMed ID: 10951463
[TBL] [Abstract][Full Text] [Related]
3. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
Huang XL; de Michelena MI; Mark H; Harston R; Benke PJ; Price SJ; Milunsky A
Clin Genet; 2005 Dec; 68(6):513-9. PubMed ID: 16283881
[TBL] [Abstract][Full Text] [Related]
4. Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker.
Dufke A; Walczak C; Liehr T; Starke H; Trifonov V; Rubtsov N; Schöning M; Enders H; Eggermann T
Eur J Hum Genet; 2001 Aug; 9(8):572-6. PubMed ID: 11528501
[TBL] [Abstract][Full Text] [Related]
5. Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.
Tonnies H; Gerlach A; Heineking B; Starke H; Neitzel H; Neumann LM
Cytogenet Genome Res; 2006; 114(3-4):325-9. PubMed ID: 16954674
[TBL] [Abstract][Full Text] [Related]
6. Mosaic tetrasomy 8q: inverted duplication of 8q23.3qter in an analphoid marker.
Reddy KS; Sulcova V; Schwartz S; Noble JE; Phillips J; Brasel JA; Huff K; Lin HJ
Am J Med Genet; 2000 May; 92(1):69-76. PubMed ID: 10797426
[TBL] [Abstract][Full Text] [Related]
7. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.
Mascarenhas A; Matoso E; Saraiva J; Tönnies H; Gerlach A; Julião MJ; Melo JB; Carreira IM
Cytogenet Genome Res; 2008; 121(3-4):293-7. PubMed ID: 18758175
[TBL] [Abstract][Full Text] [Related]
10. Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors.
Hu J; McPherson E; Surti U; Hasegawa SL; Gunawardena S; Gollin SM
Am J Med Genet; 2002 Nov; 113(1):82-8. PubMed ID: 12400070
[TBL] [Abstract][Full Text] [Related]
11. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
Spikes AS; Hegmann K; Smith JL; Shaffer LG
Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Pallister-Killian syndrome: tetrasomy of 12pter-->12p11.22 in a boy with an analphoid, inverted duplicated marker chromosome.
Huang XL; Isabel de Michelena M; Leon E; Maher TA; McClure R; Milunsky A
Clin Genet; 2007 Nov; 72(5):434-40. PubMed ID: 17894838
[TBL] [Abstract][Full Text] [Related]
14. Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha-satellite DNA probes: detection of a centromeric DNA break?
Cantú ES; Khan TA; Pai GS
Am J Med Genet; 1992 Oct; 44(3):340-4. PubMed ID: 1488982
[TBL] [Abstract][Full Text] [Related]
15. Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.
Li S; Malafiej P; Levy B; Mahmood R; Field M; Hughes T; Lockhart LH; Wu Z; Huang M; Hirschhorn K; Velagaleti GV; Daniel A; Warburton PE
Am J Med Genet; 2002 Jul; 110(3):258-67. PubMed ID: 12116235
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Marker chromosome 21 identified by microdissection and FISH.
Sun Y; Rubinstein J; Soukup S; Palmer CG
Am J Med Genet; 1995 Mar; 56(2):151-4. PubMed ID: 7542834
[TBL] [Abstract][Full Text] [Related]
18. Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomalies.
Van den Enden A; Verschraegen-Spae MR; Van Roy N; Decaluwe W; De Praeter C; Speleman F
Am J Med Genet; 1996 Jun; 63(3):482-5. PubMed ID: 8737657
[TBL] [Abstract][Full Text] [Related]
19. 10p duplication characterized by fluorescence in situ hybridization.
Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
[TBL] [Abstract][Full Text] [Related]
20. Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence.
Assumpção JG; Berkofsky-Fessler W; Viguetti Campos N; Trevas Maciel-Guerra A; Li S; Melaragno MI; Palandi de Mello M; Warburton PE
Am J Med Genet; 2002 Dec; 113(3):263-7. PubMed ID: 12439894
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
