Pallister-Killian syndrome (Q38271472)

1 September 2017

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title

Pallister-Killian syndrome. (English)

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1 September 2017

Kosuke Izumi

1

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1 September 2017

Ian D Krantz

series ordinal

2

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1 September 2017

publication date

25 November 2014

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American Journal of Medical Genetics Part C: Seminars in Medical Genetics

1 September 2017

published in

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1 September 2017

volume

166C

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1 September 2017

issue

4

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1 September 2017

page(s)

406-413

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Fog2 is required for normal diaphragm and lung development in mice and humans

1 September 2017

cites work

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https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister-Killian syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31423

ING4 Mediates Crosstalk between Histone H3 K4 Trimethylation and H3 Acetylation to Attenuate Cellular Transformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Submicroscopic familial chromosomal translocation between 7q and 12p mimicking an autosomal dominant holoprosencephaly syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31423

12p microRNA expression in fibroblast cell lines from probands with Pallister-Killian syndrome

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Genome-wide expression analysis in fibroblast cell lines from probands with Pallister Killian syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31423

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Role of gain of 12p in germ cell tumour development

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.C.31423

The ING4 tumor suppressor attenuates NF-kappaB activity at the promoters of target genes

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Letter: Trisomy-20 syndrome in man.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Cardiac manifestations of Pallister-Killian syndrome.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Chromatin deacetylation by an ATP-dependent nucleosome remodelling complex

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Isochromosome 12p mosaicism (Pallister-Killian syndrome): newborn diagnosis by direct bone marrow analysis.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.C.31423

Novel clinical manifestations in Pallister-Killian syndrome: comprehensive evaluation of 59 affected individuals and review of previously reported cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31423

ING4 induces G2/M cell cycle arrest and enhances the chemosensitivity to DNA-damage agents in HepG2 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31423

21 January 2018

Identifiers

DOI

10.1002/AJMG.C.31423

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1 September 2017

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