248 related articles for article (PubMed ID: 17901697)
21. Severe psychomotor retardation in a boy with a small supernumerary marker chromosome 19p.
Vraneković J; Brajenović-Milić B; Modrusan-Mozetić Z; Babić I; Kapović M
Cytogenet Genome Res; 2008; 121(3-4):298-301. PubMed ID: 18758176
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines.
Brecevic L; Michel S; Starke H; Müller K; Kosyakova N; Mrasek K; Weise A; Liehr T
Cytogenet Genome Res; 2006; 114(3-4):319-24. PubMed ID: 16954673
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face.
Sarri C; Gyftodimou Y; Grigoriadou M; Pandelia E; Kalogirou S; Kokotas H; Mrasek K; Weise A; Petersen MB
Cytogenet Genome Res; 2006; 114(3-4):330-7. PubMed ID: 16954675
[TBL] [Abstract][Full Text] [Related]
26. The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes.
Weber A; Liehr T; Al-Rikabi A; Bilgen S; Heinrich U; Schiller J; Stumm M
Biomedicines; 2022 May; 10(5):. PubMed ID: 35625839
[TBL] [Abstract][Full Text] [Related]
27. Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.
Li S; Malafiej P; Levy B; Mahmood R; Field M; Hughes T; Lockhart LH; Wu Z; Huang M; Hirschhorn K; Velagaleti GV; Daniel A; Warburton PE
Am J Med Genet; 2002 Jul; 110(3):258-67. PubMed ID: 12116235
[TBL] [Abstract][Full Text] [Related]
28. Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.
Liehr T; Mrasek K; Weise A; Dufke A; Rodríguez L; Martínez Guardia N; Sanchís A; Vermeesch JR; Ramel C; Polityko A; Haas OA; Anderson J; Claussen U; von Eggeling F; Starke H
Cytogenet Genome Res; 2006; 112(1-2):23-34. PubMed ID: 16276087
[TBL] [Abstract][Full Text] [Related]
29. Identification of supernumerary der(20) chromosomes by FISH in three patients.
Viersbach R; Engels H; Schwanitz G
Am J Med Genet; 1997 Jun; 70(3):278-83. PubMed ID: 9188666
[TBL] [Abstract][Full Text] [Related]
30. Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres - a long term in vitro study.
Hussein SS; Kreskowski K; Ziegler M; Klein E; Hamid AB; Kosyakova N; Volleth M; Liehr T; Fan X; Piaszinski K
Gene; 2014 Dec; 552(2):246-8. PubMed ID: 25245454
[TBL] [Abstract][Full Text] [Related]
31. Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient.
Liehr T; Mrasek K; Starke H; Claussen U; Schreiber G
Cytogenet Genome Res; 2005; 111(2):179-81. PubMed ID: 16103662
[TBL] [Abstract][Full Text] [Related]
32. Characterization of sSMC by FISH and molecular techniques.
Sheth F; Andrieux J; Ewers E; Kosyakova N; Weise A; Sheth H; Romana SP; LeLorc'h M; Delobel B; Theisen O; Liehr T; Nampoothiri S; Sheth J
Eur J Med Genet; 2011; 54(3):247-55. PubMed ID: 21316495
[TBL] [Abstract][Full Text] [Related]
33. Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.
Liehr T; Starke H; Senger G; Melotte C; Weise A; Vermeesch JR
Am J Med Genet A; 2006 Jan; 140(1):46-51. PubMed ID: 16333826
[TBL] [Abstract][Full Text] [Related]
34. De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic features.
Vundinti BR; Korgaonkar S; Ghosh K
Gene; 2012 Apr; 498(1):128-30. PubMed ID: 22342255
[TBL] [Abstract][Full Text] [Related]
35. Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions.
Guediche N; Tosca L; Nouchy M; Lecerf L; Cornet D; Brisset S; Goossens M; Tachdjian G
Eur J Med Genet; 2012 Dec; 55(12):737-42. PubMed ID: 23017438
[TBL] [Abstract][Full Text] [Related]
36. Characterization of a familial small supernumerary marker chromosome in a patient with adult-onset tongue cancer.
Bakshi SR; Dave BJ; Sanger W; Brahmbhatt MM; Trivedi PJ; Kakadia PM; Patel SJ
Cytogenet Genome Res; 2008; 121(1):14-7. PubMed ID: 18544921
[TBL] [Abstract][Full Text] [Related]
37. Chromothripsis Detectable in Small Supernumerary Marker Chromosomes (sSMC) Using Fluorescence In Situ Hybridization (FISH).
Liehr T
Methods Mol Biol; 2018; 1769():79-84. PubMed ID: 29564819
[TBL] [Abstract][Full Text] [Related]
38. Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization.
Lasan Trcić R; Hitrec V; Letica L; Cuk M; Begović D
Croat Med J; 2003 Aug; 44(4):477-9. PubMed ID: 12950153
[TBL] [Abstract][Full Text] [Related]
39. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18.
Chen CP; Lin CC; Su YN; Tsai FJ; Chen JT; Chern SR; Lee CC; Town DD; Chen LF; Wu PC; Wang W
Taiwan J Obstet Gynecol; 2010 Jun; 49(2):188-91. PubMed ID: 20708526
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
