387 related articles for article (PubMed ID: 17236832)
1. 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]
2. 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]
3. 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]
4. 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]
5. Ring chromosome 21 and reproductive pattern: a familial case and review of the literature.
Bertini V; Valetto A; Uccelli A; Tarantino E; Simi P
Fertil Steril; 2008 Nov; 90(5):2004.e1-5. PubMed ID: 18371955
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Another small supernumerary marker chromosome (sSMC) derived from chromosome 2: towards a genotype/phenotype correlation.
Mrasek K; Starke H; Liehr T
J Histochem Cytochem; 2005 Mar; 53(3):367-70. PubMed ID: 15750022
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Small familial supernumerary ring chromosome 2: FISH characterization and genotype-phenotype correlation.
Giardino D; Finelli P; Russo S; Gottardi G; Rodeschini O; Atza MG; Natacci F; Larizza L
Am J Med Genet; 2002 Aug; 111(3):319-23. PubMed ID: 12210331
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation.
Rossi E; Riegel M; Messa J; Gimelli S; Maraschio P; Ciccone R; Stroppi M; Riva P; Perrotta CS; Mattina T; Memo L; Baumer A; Kucinskas V; Castellan C; Schinzel A; Zuffardi O
J Med Genet; 2008 Mar; 45(3):147-54. PubMed ID: 18006671
[TBL] [Abstract][Full Text] [Related]
16. Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype.
Tan-Sindhunata G; Castedo S; Leegte B; Mulder I; vd Veen AY; vd Hout AH; Wiersma TJ; van Essen AJ
Am J Med Genet; 2000 May; 92(2):147-52. PubMed ID: 10797441
[TBL] [Abstract][Full Text] [Related]
17. Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.
Baumer A; Giovannucci Uzielli ML; Guarducci S; Lapi E; Röthlisberger B; Schinzel A
Am J Med Genet; 2002 Nov; 113(1):101-4. PubMed ID: 12400074
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Small supernumerary marker chromosomes (sSMC) - what about the genotype-phenotype correlation?
Liehr T; Kosyakova N
Tsitologiia; 2013; 55(3):165-6. PubMed ID: 23795458
[TBL] [Abstract][Full Text] [Related]
20. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
D'Amato Sizonenko L; Ng D; Oei P; Winship I
Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]