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Article

Microdeletion of 7p12.1p13, including IKZF1, causes intellectual impairment, overgrowth, and susceptibility to leukaemia.

British journal of haematology - 1 Apr 2019

Järviaho Tekla, Zachariadis Vasilios, Tesi Bianca, Chiang Samuel, Bryceson Yenan T, Möttönen Merja, Niinimäki Riitta, Bang Benedicte, Rahikkala Elisa, Taylan Fulya, Uusimaa Johanna, Harila-Saari Arja, Nordgren Ann

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Share to Chromosomes, Human, Pair 7
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 30004112
DOI: 10.1111/bjh.15494

Genes

IKZF1

Provenance

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Related research

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Microdeletion of 7p12.1p13, including IKZF1, causes intellectual impairment, overgrowth, and susceptibility to leukaemia.PMID 30004112Read ↗

Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia.Semantic proximity Read ↗

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A novel microdeletion involving the 13q31.3-q32.1 region in a patient with normal intelligence.Semantic proximity Read ↗

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Characterization of a 8q21.11 microdeletion syndrome associated with intellectual disability and a recognizable phenotype.Semantic proximity Read ↗

A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndromeSemantic proximity Read ↗

A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromes.Semantic proximity Read ↗

Molecular characterisation of a 3.5 Mb interstitial 14q deletion in a child with several phenotypic anomalies.Semantic proximity Read ↗

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Microdeletion in distal 17p13.1: a recognizable phenotype with microcephaly, distinctive facial features, and intellectual disability.Semantic proximity Read ↗

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Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes.Semantic proximity Read ↗

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