145 related articles for article (PubMed ID: 11438953)
1. 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]
2. 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]
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, characterization and clinical implications of two markers detected at prenatal diagnosis.
Leite RP; Souto M; Carvalho B; Martins M; Chaves R; Morais A; Guedes-Pinto H; Wienberg J; Ribeiro E
Prenat Diagn; 2006 Oct; 26(10):920-4. PubMed ID: 16845683
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.
Fickelscher I; Starke H; Schulze E; Ernst G; Kosyakova N; Mkrtchyan H; MacDermont K; Sebire N; Liehr T
Prenat Diagn; 2007 Aug; 27(8):783-5. PubMed ID: 17546703
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16.
Yakut S; Cetin Z; Simşek M; Karaüzüm SB; Tükün A; Lüleci G
Genet Couns; 2009; 20(4):327-32. PubMed ID: 20162867
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics.
Liehr T
Methods Mol Biol; 2008; 444():27-38. PubMed ID: 18425469
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome.
Yakut S; Cetin Z; Berker-Karauzum S; Mihci E; Mendilcioglu I; Luleci G
Genet Couns; 2011; 22(1):63-8. PubMed ID: 21614990
[TBL] [Abstract][Full Text] [Related]
16. Handling small supernumerary marker chromosomes in prenatal diagnostics.
Liehr T; Ewers E; Kosyakova N; Klaschka V; Rietz F; Wagner R; Weise A
Expert Rev Mol Diagn; 2009 May; 9(4):317-24. PubMed ID: 19435454
[TBL] [Abstract][Full Text] [Related]
17. The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey.
Karaman B; Aytan M; Yilmaz K; Toksoy G; Onal EP; Ghanbari A; Engur A; Kayserili H; Yuksel-Apak M; Basaran S
Eur J Med Genet; 2006; 49(3):207-14. PubMed ID: 16762822
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Two new cases of de novo small supernumerary marker chromosomes (sSMC) detected at prenatal diagnosis.
Jardim A; Melo JB; Matoso E; Pires LM; Ramos L; Carreira IM
Prenat Diagn; 2007 Apr; 27(4):380-1. PubMed ID: 17393554
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
