1546 related articles for article (PubMed ID: 16900777)
1. 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]
2. 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]
3. 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]
4. 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]
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. 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]
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. 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]
9. Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
Darnaude MT; Diaz de Bustamante A; Cabello P; Vallcorba I
Ann Genet; 1996; 39(2):61-3. PubMed ID: 8766134
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Use of chromosome painting for marker chromosome identification in two children with congenital disorders.
Doco-Fenzy M; Navrocki B; Cornillet P; Sabouraud P; Robillard P; Gruson N; Gaillard D; Adnet JJ
Bull Assoc Anat (Nancy); 1994 Jun; 78(241):9-13. PubMed ID: 8086666
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. M-FISH applications in clinical genetics.
Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Combined use of cytogenetic analysis and FISH for the identification of two antenatal de novo markers as Robertsonian translocations involving the p arms.
Pierluigi M; Battaglia P; Perfumo C; Baroncini A; Bricarelli FD
Ann Genet; 1997; 40(2):99-103. PubMed ID: 9259956
[TBL] [Abstract][Full Text] [Related]
17. Identification of marker chromosomes in thirteen patients using FISH probing.
Daniel A; Malafiej P; Preece K; Chia N; Nelson J; Smith M
Am J Med Genet; 1994 Oct; 53(1):8-18. PubMed ID: 7802042
[TBL] [Abstract][Full Text] [Related]
18. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. 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]
[Next] [New Search]
