325 related articles for article (PubMed ID: 8494036)
1. Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes.
Michalski K; Rauer M; Williamson N; Perszyk A; Hoo JJ
Am J Med Genet; 1993 Apr; 46(1):88-94. PubMed ID: 8494036
[TBL] [Abstract][Full Text] [Related]
2. Five cases of supernumerary small ring chromosomes 1: heterogeneity and genotype-phenotype correlation.
Bernardini L; Capalbo A; D'Avanzo MG; Torrente I; Grammatico P; Dell'Edera D; Cavalcanti DP; Novelli A; Dallapiccola B
Eur J Med Genet; 2007; 50(2):94-102. PubMed ID: 17236832
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of supernumerary ring chromosome 1: case report and review of the literature.
Wray AM; Dennis TR; Ghidini A; Gorman B; Haddad BR; Meck JM
Genet Couns; 2007; 18(2):233-41. PubMed ID: 17710876
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. The clinical application of spectral karyotyping (SKY) in the analysis of prenatally diagnosed extra structurally abnormal chromosomes (ESACs).
Yaron Y; Carmon E; Goldstein M; Voskoboinik N; Ochshorn Y; Gelman-Kohan Z; Orr-Urtreger A
Prenat Diagn; 2003 Jan; 23(1):74-9. PubMed ID: 12533818
[TBL] [Abstract][Full Text] [Related]
11. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.
Knegt AC; Li S; Engelen JJ; Bijlsma EK; Warburton PE
Prenat Diagn; 2003 Mar; 23(3):215-20. PubMed ID: 12627422
[TBL] [Abstract][Full Text] [Related]
13. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
Suzumori K; Tanemura M; Oya N; Suzumori N; Kim KC; Ohashi H; Fukushima Y
Prenat Diagn; 1998 Jul; 18(7):725-30. PubMed ID: 9706655
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: two new cases and review of the literature.
Ruiz C; Grubs RE; Jewett T; Cox-Jones K; Abruzzese E; Pettenati MJ; Rao PN
Am J Med Genet; 1996 Aug; 64(3):478-84. PubMed ID: 8862625
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Prenatal diagnosis of minute supernumerary marker chromosomes.
Cotter PD; Drexler K; Corley AL; Covert SM; Moland JS; Govberg IJ; Norton ME
Gynecol Obstet Invest; 2005; 60(1):27-38. PubMed ID: 15689640
[TBL] [Abstract][Full Text] [Related]
18. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A boy with small supernumerary marker chromosome X identified by FISH.
Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
