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Journal Abstract Search

319 related items for PubMed ID: 12082482

  • 1. 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
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  • 2. Pallister-Killian syndrome: report of one case.
    Wu HC, Lin LH, Tsai LP, Huang CH, Hung KL, Liao HT.
    Acta Paediatr Taiwan; 2006; 47(3):139-41. PubMed ID: 17078467
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  • 3. Pallister-Killian and Fryns syndromes: nosology.
    McPherson EW, Ketterer DM, Salsburey DJ.
    Am J Med Genet; 1993 Aug 15; 47(2):241-5. PubMed ID: 8213912
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  • 4. 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 Aug 15; 221(2):97-9. PubMed ID: 19067289
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  • 5. 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 01; 41(3):381-7. PubMed ID: 1789295
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  • 6. Lethal Pallister-Killian syndrome: phenotypic similarity with Fryns syndrome.
    Rodríguez JI, Garcia I, Alvarez J, Delicado A, Palacios J.
    Am J Med Genet; 1994 Nov 01; 53(2):176-81. PubMed ID: 7856644
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  • 7. 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 01; 53(3):361-4. PubMed ID: 15750020
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  • 8. 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 01; 14(10):641-3. PubMed ID: 9605253
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  • 11. Retrospective diagnosis of Pallister-Killian syndrome by CGH array.
    Delahaye A, Pipiras E, Delorme-Vincent C, Benkhalifa M, Kasakyan S, Devisme L, Wolf JP, Benzacken B.
    Fetal Diagn Ther; 2006 Nov 01; 21(6):485-8. PubMed ID: 16969000
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  • 15. Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children).
    Mathieu M, Piussan C, Thepot F, Gouget A, Lacombe D, Pedespan JM, Serville F, Fontan D, Ruffie M, Nivelon-Chevallier A, Amblard F, Chauveau P, Moirot H, Chabrolle JP, Croquette MF, Teyssier M, Plauchu H, Pelissier MC, Gilgenkrantz S, Turc-Carel C, Turleau C, Prieur M, Le Merrer M, Gonzales M, Journel H.
    Ann Genet; 1997 Nov 01; 40(1):45-54. PubMed ID: 9150850
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  • 16. Chromosomal mosaicism in the Killian/Teschler-Nicola syndrome.
    Raffel LJ, Mohandas T, Rimoin DL.
    Am J Med Genet; 1986 Aug 01; 24(4):607-11. PubMed ID: 3740095
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  • 17. Pallister Killian syndrome: unusual significant postnatal overgrowth in a girl with otherwise typical presentation.
    Frković SH, Durisević IT, Trcić RL, Sarnavka V, Gornik KC, Muzinić D, Letica L, Barić I, Begović D.
    Coll Antropol; 2010 Mar 01; 34(1):247-50. PubMed ID: 20437642
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  • 19. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J, Kimijima Y, Yamada S, Amagasa T, Saito-Ohara F.
    J Craniomaxillofac Surg; 2000 Jun 01; 28(3):165-70. PubMed ID: 10964553
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