187 related articles for article (PubMed ID: 19729914)
1. A neocentric isochromosome Yp present as additional small supernumerary marker chromosome--evidence against U-type exchange mechanism?
Sheth F; Ewers E; Kosyakova N; Weise A; Sheth J; Patil S; Ziegler M; Liehr T
Cytogenet Genome Res; 2009; 125(2):115-6. PubMed ID: 19729914
[TBL] [Abstract][Full Text] [Related]
2. Molecular cytogenetic characterization of an isodicentric Yq and a neocentric isochromosome Yp in an azoospermic male.
Jiang Y; Yue F; Wang R; Zhang H; Li L; Li L; Li S; Liu R
Mol Med Rep; 2020 Feb; 21(2):918-926. PubMed ID: 31974623
[TBL] [Abstract][Full Text] [Related]
3. Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature.
Liehr T; Utine GE; Trautmann U; Rauch A; Kuechler A; Pietrzak J; Bocian E; Kosyakova N; Mrasek K; Boduroglu K; Weise A; Aktas D
Cytogenet Genome Res; 2007; 118(1):31-7. PubMed ID: 17901697
[TBL] [Abstract][Full Text] [Related]
4. 47,X,idic(Y),inv dup(Y): a non-mosaic case of a phenotypically normal boy with two different Y isochromosomes and neocentromere formation.
Pasantes JJ; Wimmer R; Knebel S; Münch C; Kelbova C; Junge A; Kieback P; Küpferling P; Schempp W
Cytogenet Genome Res; 2012; 136(2):157-62. PubMed ID: 22286088
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Characterization by fluorescence and electron microscopy in situ hybridization of a double Y isochromosome.
Fetni R; Krabchi K; Messier PE; Richer CL; Lemieux N
Am J Med Genet; 1996 Jun; 63(3):454-7. PubMed ID: 8737651
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Prenatal detection of isochromosome 21 by QF-PCR. A comparison between FISH and traditional karyotyping.
Gole L; Lian NB; Lian NP; Rauff M; Biswas A; Choolani M
Fetal Diagn Ther; 2008; 24(1):47-50. PubMed ID: 18504381
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.
Liehr T; Mrasek K; Hinreiner S; Reich D; Ewers E; Bartels I; Seidel J; Emmanuil N; Petesen M; Polityko A; Dufke A; Iourov I; Trifonov V; Vermeesch J; Weise A
Sex Dev; 2007; 1(6):353-62. PubMed ID: 18391547
[TBL] [Abstract][Full Text] [Related]
14. [Case reports of patients with a marker chromosome].
Kocárek E; Novotná D; Maríková T; Cernáková I; Losan F; Balícek P; Baxová A; Havlovicová M; Goetz P
Cas Lek Cesk; 2004; 143(10):708-11; discussion 711-2. PubMed ID: 15584624
[TBL] [Abstract][Full Text] [Related]
15. New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank.
Tönnies H; Pietrzak J; Bocian E; MacDermont K; Kuechler A; Belitz B; Trautmann U; Schmidt A; Schulze B; Rodríguez L; Binkert F; Yardin C; Kosyakova N; Volleth M; Mkrtchyan H; Schreyer I; von Eggeling F; Weise A; Mrasek K; Liehr T
J Histochem Cytochem; 2007 Jun; 55(6):651-60. PubMed ID: 17341473
[TBL] [Abstract][Full Text] [Related]
16. Isochromosome of Yp in a man with Sertoli-cell-only syndrome.
Lin YH; Chuang L; Lin YM; Lin YH; Teng YN; Kuo PL
Fertil Steril; 2005 Mar; 83(3):764-6. PubMed ID: 15749513
[TBL] [Abstract][Full Text] [Related]
17. Autism and hypoplastic corpus callosum in a case of monocentric marker chromosome 15.
Jovanović-Privrodski JD; Kavecan II; Obrenović MR; Buonadonna LA; Bukvić NM
Pediatr Neurol; 2009 Jul; 41(1):65-7. PubMed ID: 19520280
[TBL] [Abstract][Full Text] [Related]
18. Constitutional tetrasomy 18p.
Bakshi SR; Brahmbhatt MM; Trivedi PJ; Chudoba I
Indian Pediatr; 2006 Apr; 43(4):357-60. PubMed ID: 16651677
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Investigation of a rare supernumerary i(Y)(q10) chromosome in a patient with premature ovarian failure].
Zeng H; Kong H; Xiao Y; Huang T; Wu H; Shen Y; Zhou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Apr; 31(2):192-5. PubMed ID: 24711030
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
