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- Pallister–Killian_syndrome abstract "Pallister–Killian syndrome (also tetrasomy 12p mosaicism or Pallister mosaic aneuploidy syndrome) is an extremely rare genetic disorder occurring in humans. Pallister-Killian occurs due to the presence of the anomalous extra isochromosome 12p, the short arm of the twelfth chromosome. This leads to the development of tetrasomy 12p. Because not all cells have the extra isochromosome, Pallister-Killian is a mosaic condition.It was first described by Philip Pallister in 1977 and further researched by Maria Teschler-Nicola and Wolfgang Killian in 1981.".
- Pallister–Killian_syndrome icd10 "Q99.8".
- Pallister–Killian_syndrome icd9 "758.5".
- Pallister–Killian_syndrome omim "601803".
- Pallister–Killian_syndrome wikiPageExternalLink pks_support.
- Pallister–Killian_syndrome wikiPageExternalLink www.pkskids.net.
- Pallister–Killian_syndrome wikiPageID "5374045".
- Pallister–Killian_syndrome wikiPageLength "5688".
- Pallister–Killian_syndrome wikiPageOutDegree "40".
- Pallister–Killian_syndrome wikiPageRevisionID "679006231".
- Pallister–Killian_syndrome wikiPageWikiLink Adolescence.
- Pallister–Killian_syndrome wikiPageWikiLink Adolescent.
- Pallister–Killian_syndrome wikiPageWikiLink Amniotic_sac.
- Pallister–Killian_syndrome wikiPageWikiLink Cataract.
- Pallister–Killian_syndrome wikiPageWikiLink Category:Chromosomal_abnormalities.
- Pallister–Killian_syndrome wikiPageWikiLink Category:Disturbances_of_human_pigmentation.
- Pallister–Killian_syndrome wikiPageWikiLink Category:Rare_diseases.
- Pallister–Killian_syndrome wikiPageWikiLink Category:Syndromes.
- Pallister–Killian_syndrome wikiPageWikiLink Chorionic_villi.
- Pallister–Killian_syndrome wikiPageWikiLink Chromosome_12_(human).
- Pallister–Killian_syndrome wikiPageWikiLink Congenital.
- Pallister–Killian_syndrome wikiPageWikiLink Congenital_disorder.
- Pallister–Killian_syndrome wikiPageWikiLink Congenital_heart_defect.
- Pallister–Killian_syndrome wikiPageWikiLink Contracture.
- Pallister–Killian_syndrome wikiPageWikiLink Developmental_disability.
- Pallister–Killian_syndrome wikiPageWikiLink Epicanthal_fold.
- Pallister–Killian_syndrome wikiPageWikiLink Epicanthic_fold.
- Pallister–Killian_syndrome wikiPageWikiLink Epilepsy.
- Pallister–Killian_syndrome wikiPageWikiLink Fibroblast.
- Pallister–Killian_syndrome wikiPageWikiLink Fibroblasts.
- Pallister–Killian_syndrome wikiPageWikiLink Gastroesophageal_reflux_disease.
- Pallister–Killian_syndrome wikiPageWikiLink Genetic_disorder.
- Pallister–Killian_syndrome wikiPageWikiLink Heart_defect.
- Pallister–Killian_syndrome wikiPageWikiLink Hernia.
- Pallister–Killian_syndrome wikiPageWikiLink Human.
- Pallister–Killian_syndrome wikiPageWikiLink Hyperpigmentation.
- Pallister–Killian_syndrome wikiPageWikiLink Hypertelorism.
- Pallister–Killian_syndrome wikiPageWikiLink Hypertonia.
- Pallister–Killian_syndrome wikiPageWikiLink Hypopigmentation.
- Pallister–Killian_syndrome wikiPageWikiLink Hypotonia.
- Pallister–Killian_syndrome wikiPageWikiLink Isochromosome.
- Pallister–Killian_syndrome wikiPageWikiLink List_of_cutaneous_conditions.
- Pallister–Killian_syndrome wikiPageWikiLink Lymphocyte.
- Pallister–Killian_syndrome wikiPageWikiLink Lymphocytes.
- Pallister–Killian_syndrome wikiPageWikiLink Macroglossia.
- Pallister–Killian_syndrome wikiPageWikiLink Maria_Teschler-Nicola.
- Pallister–Killian_syndrome wikiPageWikiLink Mosaic_(genetics).
- Pallister–Killian_syndrome wikiPageWikiLink Nondisjunction.
- Pallister–Killian_syndrome wikiPageWikiLink Philip_Pallister.
- Pallister–Killian_syndrome wikiPageWikiLink Polyhydramnios.
- Pallister–Killian_syndrome wikiPageWikiLink Psychomotor_retardation.
- Pallister–Killian_syndrome wikiPageWikiLink Supernumerary_nipple.
- Pallister–Killian_syndrome wikiPageWikiLink Tetrasomy.
- Pallister–Killian_syndrome wikiPageWikiLink Thoracic_diaphragm.
- Pallister–Killian_syndrome wikiPageWikiLink Wolfgang_Killian.
- Pallister–Killian_syndrome wikiPageWikiLinkText "Pallister–Killian syndrome".
- Pallister–Killian_syndrome wikiPageWikiLinkText "Teschler-Nicola syndrome".
- Pallister–Killian_syndrome hasPhotoCollection Pallister–Killian_syndrome.
- Pallister–Killian_syndrome icd "758.5".
- Pallister–Killian_syndrome icd "Q99.8".
- Pallister–Killian_syndrome name "Pallister-Killian syndrome".
- Pallister–Killian_syndrome omim "601803".
- Pallister–Killian_syndrome wikiPageUsesTemplate Template:Chromosomal_abnormalities.
- Pallister–Killian_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Pallister–Killian_syndrome wikiPageUsesTemplate Template:Reflist.
- Pallister–Killian_syndrome wikiPageUsesTemplate Template:Unreferenced_section.
- Pallister–Killian_syndrome subject Category:Chromosomal_abnormalities.
- Pallister–Killian_syndrome subject Category:Disturbances_of_human_pigmentation.
- Pallister–Killian_syndrome subject Category:Rare_diseases.
- Pallister–Killian_syndrome subject Category:Syndromes.
- Pallister–Killian_syndrome type Disease.
- Pallister–Killian_syndrome type Thing.
- Pallister–Killian_syndrome type Q12136.
- Pallister–Killian_syndrome comment "Pallister–Killian syndrome (also tetrasomy 12p mosaicism or Pallister mosaic aneuploidy syndrome) is an extremely rare genetic disorder occurring in humans. Pallister-Killian occurs due to the presence of the anomalous extra isochromosome 12p, the short arm of the twelfth chromosome. This leads to the development of tetrasomy 12p.".
- Pallister–Killian_syndrome label "Pallister–Killian syndrome".
- Pallister–Killian_syndrome sameAs Pallister-Killian-Syndrom.
- Pallister–Killian_syndrome sameAs Síndrome_de_Pallister-Killian.
- Pallister–Killian_syndrome sameAs Pallister–Killianin_oireyhtymä.
- Pallister–Killian_syndrome sameAs Sindrome_di_Pallister-Killian.
- Pallister–Killian_syndrome sameAs m.0dhzvd.
- Pallister–Killian_syndrome sameAs Q1425018.
- Pallister–Killian_syndrome sameAs Q1425018.
- Pallister–Killian_syndrome wasDerivedFrom Pallister–Killian_syndrome?oldid=679006231.
- Pallister–Killian_syndrome isPrimaryTopicOf Pallister–Killian_syndrome.
- Pallister–Killian_syndrome name "Pallister-Killian syndrome".