These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
105 related articles for article (PubMed ID: 22166535)
1. Pallister-Killian syndrome: meiosis II non-disjunction may be the first step in the formation of isochromosome 12p. Shen JD; Liang DS; Zhou ZM; Xia Y; Long ZG; Wu LQ Chin Med J (Engl); 2010 Dec; 123(23):3482-5. PubMed ID: 22166535 [No Abstract] [Full Text] [Related]
2. Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister-Killian syndrome. Conlin LK; Kaur M; Izumi K; Campbell L; Wilkens A; Clark D; Deardorff MA; Zackai EH; Pallister P; Hakonarson H; Spinner NB; Krantz ID Am J Med Genet A; 2012 Dec; 158A(12):3046-53. PubMed ID: 23169773 [TBL] [Abstract][Full Text] [Related]
3. Post-zygotic origin of isochromosome 12p. de Ravel TJ; Keymolen K; van Assche E; Wittevronghel I; Moerman P; Salden I; Matthijs G; Fryns JP; Vermeesch JR Prenat Diagn; 2004 Dec; 24(12):984-8. PubMed ID: 15614858 [TBL] [Abstract][Full Text] [Related]
4. Pallister-Killian syndrome: rapid decrease of isochromosome 12p frequency during amniocyte subculturing. Conclusion for strategy of prenatal cytogenetic diagnostics. Polityko AD; Goncharova E; Shamgina L; Drozdovskaja N; Podleschuk L; Abramchik E; Jaroshevich E; Khurs O; Pisarik I; Pribushenya O; Rumyantseva N; Naumchik I J Histochem Cytochem; 2005 Mar; 53(3):361-4. PubMed ID: 15750020 [TBL] [Abstract][Full Text] [Related]
5. Pallister-Killian syndrome. Izumi K; Krantz ID Am J Med Genet C Semin Med Genet; 2014 Dec; 166C(4):406-13. PubMed ID: 25425112 [TBL] [Abstract][Full Text] [Related]
6. Supernumerary ring chromosome: an etiology for Pallister-Killian syndrome? Lloveras E; Canellas A; Cirigliano V; CatalĂ V; Cerdan C; Plaja A Fetal Diagn Ther; 2013; 34(3):172-5. PubMed ID: 23485930 [TBL] [Abstract][Full Text] [Related]
7. Phenotypic overlapping of trisomy 12p and Pallister-Killian syndrome. Inage E; Suzuki M; Minowa K; Akimoto N; Hisata K; Shoji H; Okumura A; Shimojima K; Shimizu T; Yamamoto T Eur J Med Genet; 2010; 53(3):159-61. PubMed ID: 20219705 [TBL] [Abstract][Full Text] [Related]
8. Report of two new cases of Pallister-Killian syndrome confirmed by FISH: tissue-specific mosaicism and loss of i(12p) by in vitro selection. Schubert R; Viersbach R; Eggermann T; Hansmann M; Schwanitz G Am J Med Genet; 1997 Oct; 72(1):106-10. PubMed ID: 9295085 [TBL] [Abstract][Full Text] [Related]
9. Parental origin of the isochromosome 12p in Pallister-Killian syndrome: molecular analysis of one patient and review of the reported cases. Struthers JL; Cuthbert CD; Khalifa MM Am J Med Genet; 1999 May; 84(2):111-5. PubMed ID: 10323734 [TBL] [Abstract][Full Text] [Related]
10. Pallister-Killian Syndrome (PKS) as a Cause of Mental Retardation. Shamdeen A; Meyer S; Gottschling S; Oehl-Jaschkowitz B; Gortner L; Shamdeen MG Klin Padiatr; 2009; 221(2):97-9. PubMed ID: 19067289 [TBL] [Abstract][Full Text] [Related]
11. 12p microRNA expression in fibroblast cell lines from probands with Pallister-Killian syndrome. Izumi K; Zhang Z; Kaur M; Krantz ID Chromosome Res; 2014 Dec; 22(4):453-61. PubMed ID: 24981202 [TBL] [Abstract][Full Text] [Related]
12. [Tetrasomy 12p (Pallister-Killian syndrome): possible diagnosis before the age of a year]. Chrzanowska K; Fryns JP J Genet Hum; 1989 Sep; 37(3):259-61. PubMed ID: 2625629 [TBL] [Abstract][Full Text] [Related]
13. Pallister-Killian syndrome: case report with pineal tumor. Mauceri L; Sorge G; Incorpora G; Pavone L Am J Med Genet; 2000 Nov; 95(1):75-8. PubMed ID: 11074499 [TBL] [Abstract][Full Text] [Related]
14. The Pallister-Killian syndrome in an African individual. Woodman BF; Jordan MA; Moller LI; Cartwright JD; De Ravel TJ Genet Couns; 1995; 6(1):33-6. PubMed ID: 7794559 [TBL] [Abstract][Full Text] [Related]
15. Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome. Cormier-Daire V; Le Merrer M; Gigarel N; Morichon N; Prieur M; Lyonnet S; Vekemans M; Munnich A Am J Med Genet; 1997 Mar; 69(2):166-8. PubMed ID: 9056554 [TBL] [Abstract][Full Text] [Related]
16. An Indian boy with additional features in Pallister-Killian syndrome. Shah K; George R; Balla ES; Oommen SP; Padankatti CS; Srivastava VM; Danda S Indian J Pediatr; 2012 Sep; 79(9):1238-40. PubMed ID: 22012142 [TBL] [Abstract][Full Text] [Related]
17. Duplication 12p and Pallister-Killian syndrome: a case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region. Izumi K; Conlin LK; Berrodin D; Fincher C; Wilkens A; Haldeman-Englert C; Saitta SC; Zackai EH; Spinner NB; Krantz ID Am J Med Genet A; 2012 Dec; 158A(12):3033-45. PubMed ID: 23169682 [TBL] [Abstract][Full Text] [Related]
19. Genome-wide expression analysis in fibroblast cell lines from probands with Pallister Killian syndrome. Kaur M; Izumi K; Wilkens AB; Chatfield KC; Spinner NB; Conlin LK; Zhang Z; Krantz ID PLoS One; 2014; 9(10):e108853. PubMed ID: 25329894 [TBL] [Abstract][Full Text] [Related]
20. A case of mosaic tetrasomy 12p (Pallister-Killian Syndrome) diagnosed prenatally: comparison of chromosome analyses of various cells obtained from the patient. Takakuwa K; Hataya I; Arakawa M; Tamura M; Sekizuka N; Tanaka K Am J Perinatol; 1997 Nov; 14(10):641-3. PubMed ID: 9605253 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]