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 *

174 related articles for article (PubMed ID: 18000900)

  • 1. Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNA.
    Powis Z; Kang SH; Cooper ML; Patel A; Peiffer DA; Hawkins A; Heidenreich R; Gunderson KL; Cheung SW; Erickson RP
    Am J Med Genet A; 2007 Dec; 143A(24):2910-5. PubMed ID: 18000900
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.
    Chen CP; Peng CR; Chern SR; Kuo YL; Wu PS; Town DD; Pan CW; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):566-71. PubMed ID: 25510702
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pallister-Killian syndrome caused by mosaicism for a supernumerary ring chromosome 12p.
    Yeung A; Francis D; Giouzeppos O; Amor DJ
    Am J Med Genet A; 2009 Mar; 149A(3):505-9. PubMed ID: 19215037
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pallister-Killian syndrome in a girl with mild developmental delay and mosaicism for hexasomy 12p.
    Vogel I; Lyngbye T; Nielsen A; Pedersen S; Hertz JM
    Am J Med Genet A; 2009 Mar; 149A(3):510-4. PubMed ID: 19215056
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):852-856. PubMed ID: 29241934
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis.
    Libotte F; Bizzoco D; Gabrielli I; Mesoraca A; Cignini P; Vitale SG; Marilli I; Gulino FA; Rapisarda AM; Giorlandino C
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):863-866. PubMed ID: 28040135
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.
    Horn D; Majewski F; Hildebrandt B; Körner H
    J Med Genet; 1995 Jan; 32(1):68-71. PubMed ID: 7897632
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Postnatal clinical phenotype of five patients with Pallister-Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature.
    Alqahtani AS; Putoux A; Bonnet Dupeyron MN; Carneiro M; Lion-Francois L; Rossi M; Tevissen H; Schluth Bolard C; Labalme A; Lesca G; Till M; Edery P; Sanlaville D
    Mol Genet Genomic Med; 2019 Oct; 7(10):e00939. PubMed ID: 31454185
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Array CGH on unstimulated blood does not detect all cases of Pallister-Killian syndrome: a skin biopsy should remain the diagnostic gold standard.
    Hodge JC; Hulshizer RL; Seger P; St Antoine A; Bair J; Kirmani S
    Am J Med Genet A; 2012 Mar; 158A(3):669-73. PubMed ID: 22315202
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lethal presentation of mosaic tetrasomy 12p (Pallister-Killian) syndrome.
    Young ID; Duckett DP; O'Reilly KM
    Ann Genet; 1989; 32(1):62-4. PubMed ID: 2751252
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. aCGH detects partial tetrasomy of 12p in blood from Pallister-Killian syndrome cases without invasive skin biopsy.
    Theisen A; Rosenfeld JA; Farrell SA; Harris CJ; Wetzel HH; Torchia BA; Bejjani BA; Ballif BC; Shaffer LG
    Am J Med Genet A; 2009 May; 149A(5):914-8. PubMed ID: 19353629
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Polymicrogyria with calcification in Pallister-Killian syndrome detected by microarray analysis.
    Hiraiwa A; Matsui K; Nakayama Y; Komatsubara T; Magara S; Kobayashi Y; Hojo M; Kato M; Yamamoto T; Tohyama J
    Brain Dev; 2021 Mar; 43(3):448-453. PubMed ID: 33229101
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Using Array-Based Comparative Genomic Hybridization to Diagnose Pallister-Killian Syndrome.
    Lee MN; Lee J; Yu HJ; Lee J; Kim SH
    Ann Lab Med; 2017 Jan; 37(1):66-70. PubMed ID: 27834069
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tetrasomy 12p (Pallister-Killian syndrome): ultrasound indicators and confirmation by interphase fish.
    Wilson RD; Harrison K; Clarke LA; Yong SL
    Prenat Diagn; 1994 Sep; 14(9):787-92. PubMed ID: 7845885
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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; 21(6):485-8. PubMed ID: 16969000
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A further prenatal diagnosis of mosaic tetrasomy 12p (Pallister-Killian syndrome).
    Tejada MI; Uribarren A; Briones P; Vilaseca MA
    Prenat Diagn; 1992 Jun; 12(6):529-34. PubMed ID: 1513756
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pallister-Killian syndrome: a study of 22 British patients.
    Blyth M; Maloney V; Beal S; Collinson M; Huang S; Crolla J; Temple IK; Baralle D
    J Med Genet; 2015 Jul; 52(7):454-64. PubMed ID: 25888713
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.