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9. [Mosaic tetrasomy 12p. Identical nature of the Pallister syndrome, the Teschler-Nicola/Killian syndrome and mosaic tetrasomy 21]. Gilgenkrantz S; Fryns JP; Droulle P; Schweitzer M; Chadefaux B; Prieur M J Genet Hum; 1987 Jan; 35(1):51-61. PubMed ID: 3559524 [TBL] [Abstract][Full Text] [Related]
10. Tissue-limited mosaicism in Pallister-Killian syndrome -- a case in point. Choo S; Teo SH; Tan M; Yong MH; Ho LY J Perinatol; 2002; 22(5):420-3. PubMed ID: 12082482 [TBL] [Abstract][Full Text] [Related]
11. Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes. Pauli S; Schmidt T; Funke R; Zoll B; Burfeind P; Dybowski U; Shoukier M; Bartels I Eur J Med Genet; 2012; 55(8-9):480-4. PubMed ID: 22677035 [TBL] [Abstract][Full Text] [Related]
12. Clinical, cytogenetic, and molecular observations in a patient with Pallister-Killian-syndrome with an unusual karyotype. Leube B; Majewski F; Gebauer J; Royer-Pokora B Am J Med Genet A; 2003 Dec; 123A(3):296-300. PubMed ID: 14608653 [TBL] [Abstract][Full Text] [Related]
13. Retinal pigment mosaicism in Pallister-Killian syndrome (mosaic tetrasomy 12p). Graham W; Brown SM; Shah F; Tonk VS; Kukolich MK Arch Ophthalmol; 1999 Dec; 117(12):1648-9. PubMed ID: 10604674 [No Abstract] [Full Text] [Related]
14. [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]
15. 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]
16. Pericardial agenesis and focal aplasia cutis in tetrasomy 12p (Pallister-Killian syndrome). Zakowski MF; Wright Y; Ricci A Am J Med Genet; 1992 Feb; 42(3):323-5. PubMed ID: 1536171 [TBL] [Abstract][Full Text] [Related]
17. Trisomy 8: an international study of 70 patients. Riccardi VM Birth Defects Orig Artic Ser; 1977; 13(3C):171-84. PubMed ID: 890109 [TBL] [Abstract][Full Text] [Related]
19. Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridization. Speleman F; Leroy JG; Van Roy N; De Paepe A; Suijkerbuijk R; Brunner H; Looijenga L; Verschraegen-Spae MR; Orye E Am J Med Genet; 1991 Dec; 41(3):381-7. PubMed ID: 1789295 [TBL] [Abstract][Full Text] [Related]
20. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases. Reynolds JF; Daniel A; Kelly TE; Gollin SM; Stephan MJ; Carey J; Adkins WN; Webb MJ; Char F; Jimenez JF Am J Med Genet; 1987 Jun; 27(2):257-74. PubMed ID: 3605212 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]