150 related articles for article (PubMed ID: 15508017)
1. Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited.
Crolla JA; Youings SA; Ennis S; Jacobs PA
Eur J Hum Genet; 2005 Feb; 13(2):154-60. PubMed ID: 15508017
[TBL] [Abstract][Full Text] [Related]
2. FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature.
Crolla JA
Am J Med Genet; 1998 Feb; 75(4):367-81. PubMed ID: 9482642
[TBL] [Abstract][Full Text] [Related]
3. Supernumerary marker chromosomes detected in 100,000 prenatal diagnoses: molecular cytogenetic studies and clinical significance.
Huang B; Solomon S; Thangavelu M; Peters K; Bhatt S
Prenat Diagn; 2006 Dec; 26(12):1142-50. PubMed ID: 17009345
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Characterisation of supernumerary chromosomal markers: a study of 13 cases.
Douet-Guilbert N; Marical H; Pinson L; Herry A; Le Bris MJ; Morel F; De Braekeleer M
Cytogenet Genome Res; 2007; 116(1-2):18-23. PubMed ID: 17268173
[TBL] [Abstract][Full Text] [Related]
6. Forty-two supernumerary marker chromosomes (SMCs) in 43,273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies.
Bartsch O; Loitzsch A; Kozlowski P; Mazauric ML; Hickmann G
Eur J Hum Genet; 2005 Nov; 13(11):1192-204. PubMed ID: 16077735
[TBL] [Abstract][Full Text] [Related]
7. [Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics].
Douet-Guilbert N; Basinko A; Le Bris MJ; Herry A; Morel F; De Braekeleer M
Pathol Biol (Paris); 2008 Sep; 56(6):362-7. PubMed ID: 18456432
[TBL] [Abstract][Full Text] [Related]
8. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
Bartsch O; Rasi S; Hoffmann K; Blin N
Eur J Hum Genet; 2005 May; 13(5):592-8. PubMed ID: 15756300
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis.
Li MM; Howard-Peebles PN; Killos LD; Fallon L; Listgarten E; Stanley WS
Prenat Diagn; 2000 Feb; 20(2):138-43. PubMed ID: 10694686
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion of uniparental disomy for chromosome 15.
Cotter PD; Ledesma CT; Dietz LG; Pusso S; Wohlferd MM; Goldberg JD
Prenat Diagn; 1999 Aug; 19(8):721-6. PubMed ID: 10451515
[TBL] [Abstract][Full Text] [Related]
12. Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.
Santos M; Mrasek K; Rigola MA; Starke H; Liehr T; Fuster C
Fertil Steril; 2007 Oct; 88(4):969.e11-7. PubMed ID: 17451694
[TBL] [Abstract][Full Text] [Related]
13. FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases.
Crolla JA; Long F; Rivera H; Dennis NR
Am J Med Genet; 1998 Feb; 75(4):355-66. PubMed ID: 9482641
[TBL] [Abstract][Full Text] [Related]
14. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16.
Hengstschläger M; Bettelheim D; Drahonsky R; Deutinger J; Bernaschek G
Prenat Diagn; 2001 Jun; 21(6):477-80. PubMed ID: 11438953
[TBL] [Abstract][Full Text] [Related]
16. Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.
Starke H; Nietzel A; Weise A; Heller A; Mrasek K; Belitz B; Kelbova C; Volleth M; Albrecht B; Mitulla B; Trappe R; Bartels I; Adolph S; Dufke A; Singer S; Stumm M; Wegner RD; Seidel J; Schmidt A; Kuechler A; Schreyer I; Claussen U; von Eggeling F; Liehr T
Hum Genet; 2003 Dec; 114(1):51-67. PubMed ID: 13680362
[TBL] [Abstract][Full Text] [Related]
17. Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization.
Manolakos E; Kefalas K; Neroutsou R; Lagou M; Kosyakova N; Ewers E; Ziegler M; Weise A; Tsoplou P; Rapti SM; Papoulidis I; Anastasakis E; Garas A; Sotiriou S; Eleftheriades M; Peitsidis P; Malathrakis D; Thomaidis L; Kitsos G; Orru S; Liehr T; Petersen MB; Kitsiou-Tzeli S
Mol Med Rep; 2010; 3(6):1015-22. PubMed ID: 21472348
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. De novo small supernumerary marker chromosomes detected on 143,000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches.
Malvestiti F; De Toffol S; Grimi B; Chinetti S; Marcato L; Agrati C; Di Meco AM; Frascoli G; Trotta A; Malvestiti B; Ruggeri A; Dulcetti F; Maggi F; Simoni G; Grati FR
Prenat Diagn; 2014 May; 34(5):460-8. PubMed ID: 24436202
[TBL] [Abstract][Full Text] [Related]
20. Small marker chromosome mosaicism confirmed in two cases ascertained prenatally.
Kohn G; Shaham M; Ornoy A; Beyth Y; Cohen MM
Am J Med Genet; 1978; 2(2):167-73. PubMed ID: 299455
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
