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The characteristic physiognomy and tissue specific karyotype distribution in the Pallister-Killian syndrome

  • Published:2008-04-23 Issue:1 Volume:28 Page:47-53
  • ISSN:0009-9163
  • Container-title:Clinical Genetics
  • language:en
  • Short-container-title:

Author:

Hunter Alasdair G. W.,Clifford Brian,Cox David M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference17 articles.

1. “Killian syndrome” Pallister mosaic syndrome, or mosaic tetrasomy 12p? - an analysis;Buyse;J. Clin. Dysmorphol.,1983

2. Mosaic tetrasomy 21 in severe mental handicap;Fryns;Eur. J. Pediatr.,1982

3. Teschler-Nicola/Killian Syndrome: A sporadic case in an 11-year-old male;Hall;J. Clin. Dysmorphol.,1983

4. Teschler-Nicola/Killian Syndrome: A case report;Hersh;J. Clin. Dysmorph.,1983

5. Mosaic tetrasomy 21 in a liveborn male infant;Hunter;Clin. Genet.,1982

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2. PALLISTER–KILLIAN SYNDROME;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30

3. Seizures and Cardiomyopathy in a Patient with Pallister-Killian Syndrome due to Hexasomy 12p Mosaicism;Molecular Syndromology;2020

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