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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

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  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. J Ultrasound Med 2006; 25(11): 1475-1480.10.7863/jum.2006.25.11.1475
  3. Langford K, Hodgson S, Seller M, Maxwell D. Pallister-Killian syndrome presenting through nuchal translucency screening for trisomy 21. Prenat Diagn 2000; 20(8): 670-672.10.1002/1097-0223(200008)20:8<;670::AID-PD885>3.0.CO;2-U
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  5. Liehr T. Homepage on small supernumerary marker chromosomes (sSMC). http://www.med.uni-jena.de/fish/sSMC/00START.htm
  6. Liehr T. Homepage on small supernumerary marker chromosomes (sSMC) sub-page for PKS. http://www.med.uni-jena.de/fish/sSMC/12.htm#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. Am J Med Genet A 2007; 143A(24): 2910-2915.10.1002/ajmg.a.31959
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
Publication frequency: 2 times per year

© 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.

Volume 11 (2008): Issue 2 (December 2008)