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Pallister-Killian Syndrome: Rare Phenotypic Features and Variable Karyotypes Cover

Pallister-Killian Syndrome: Rare Phenotypic Features and Variable Karyotypes

Open Access
|May 2009

References

  1. Liberati M, Melchiorre K, D'Emilio I, Guanciali-Franchi PE, Iezzi I, Rotmensch S, Celentano C. Fetal facial profile in Pallister-Killian syndrome.2008; 23(1): 15-17.
  2. Abad DE, Gabarre JA, Izquierdo AM, López-Sánchez C, García-Martínez V, Izquierdo AG. Pallister-Killian syndrome presenting with a complex congenital heart defect and increased nuchal translucency.2006; 25(11): 1475-1480.
  3. Langford K, Hodgson S, Seller M, Maxwell D. Pallister-Killian syndrome presenting through nuchal translucency screening for trisomy 21.2000; 20(8): 670-672.
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  5. Liehr T. Homepage on small supernumerary marker chromosomes (sSMC).
  6. Liehr T. Homepage on small supernumerary marker chromosomes (sSMC) sub-page for PKS.
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  8. Powis Z, Kang SH, Cooper ML, Patel A, Peiffer DA, Hawkins A, Heidenreich R, Gunderson KL, Cheung SW, Erickson RP. Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNA.2007;(24): 2910-2915.
DOI: https://doi.org/10.2478/v10034-008-0023-z | Journal eISSN: 2199-5761 (formerly 1311-0160) | Journal ISSN: 1311-0160
Language: English
Page range: 65 - 67
Published on: May 6, 2009
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services

© 2009 T Liehr, R-D Wegner, M Stumm, G Joksić, A Polityko, N Kosyakova, E Ewers, D Reich, R Wagner, A Weise, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons License.