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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

76 related articles for article (PubMed ID: 20440740)

  • 1. Comment on 'genetic considerations in the prenatal diagnosis of overgrowth syndromes', by Vora and Bianchi.
    Witters I; Fryns JP
    Prenat Diagn; 2010 May; 30(5):492. PubMed ID: 20440740
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Prenatal diagnosis of trisomy 12 mosaicism: normal development of a 3 years old female child.
    Staals JE; Schrander-Stumpel CT; Hamers G; Fryns JP
    Genet Couns; 2003; 14(2):233-7. PubMed ID: 12872819
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Overgrowth. Section VI. Genetic syndromes and other disorders associated with overgrowth.
    Sotos JF
    Clin Pediatr (Phila); 1997 Mar; 36(3):157-70. PubMed ID: 9078418
    [No Abstract]   [Full Text] [Related]  

  • 6. Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome.
    Flori E; Girodon E; Samama B; Becmeur F; Viville B; Girard-Lemaire F; Doray B; Schluth C; Marcellin L; Boehm N; Goossens M; Pingault V
    Eur J Hum Genet; 2005 Sep; 13(9):1013-8. PubMed ID: 15915162
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Growth analysis in clinical genetics.
    Opitz JM; Mendez HM; Hall JG
    Prog Clin Biol Res; 1985; 200():33-63. PubMed ID: 3909165
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Trisomy 18 mosaicism in a mildly retarded boy with postnatal overgrowth.
    Plessis G; Le Treust M; Lemaire F; Maugard T; Cau D
    Ann Genet; 1997; 40(4):235-7. PubMed ID: 9526621
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case of trisomy 12 mosaicism with pituitary malformation and polycystic ovary syndrome.
    Boulard S; Diene G; Barat R; Oliver I; Pienkowski C; Lacombe D; Vincent MC; Bourrouillou G; Tauber M
    Genet Couns; 2006; 17(2):173-83. PubMed ID: 16970035
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pallister-Killian syndrome: Multiband FISH of tetrasomy 12p.
    Gerdes AM; Hansen LK; Brandrup F; Soegaard K; Christoffersen A; Rasmussen K
    Pediatr Dermatol; 2006; 23(4):378-81. PubMed ID: 16918638
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis.
    Chen CP; Chang TY; Chern SR; Lee CC; Town DD; Lee MS; Wang W
    Prenat Diagn; 2007 Apr; 27(4):383-5. PubMed ID: 17393556
    [No Abstract]   [Full Text] [Related]  

  • 13. The importance of aneuploidy screening in reciprocal translocation carriers.
    Pujol A; Benet J; Staessen C; Van Assche E; Campillo M; Egozcue J; Navarro J
    Reproduction; 2006 Jun; 131(6):1025-35. PubMed ID: 16735542
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiplex ligation-dependent probe amplification (MLPA) in prenatal diagnosis-experience of a large series of rapid testing for aneuploidy of chromosomes 13, 18, 21, X, and Y.
    Gerdes T; Kirchhoff M; Lind AM; Vestergaard Larsen G; Kjaergaard S
    Prenat Diagn; 2008 Dec; 28(12):1119-25. PubMed ID: 19003800
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of Pallister-Killian syndrome.
    Soukup S; Neidich K
    Am J Med Genet; 1990 Apr; 35(4):526-8. PubMed ID: 1692181
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification, characterization and clinical implications of two markers detected at prenatal diagnosis.
    Leite RP; Souto M; Carvalho B; Martins M; Chaves R; Morais A; Guedes-Pinto H; Wienberg J; Ribeiro E
    Prenat Diagn; 2006 Oct; 26(10):920-4. PubMed ID: 16845683
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture.
    Harrison K; Eisenger K; Anyane-Yeboa K; Brown S
    Am J Med Genet; 1995 Aug; 58(2):147-51. PubMed ID: 8533806
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pallister-Killian syndrome--an update of a clinical case.
    Wyatt PR
    Am J Med Genet; 1988 Jan; 29(1):229. PubMed ID: 3344773
    [No 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]
    of 4.