Homozygous deletion of FMS in a patient with the 5q- syndrome.

doi:10.1111/j.1365-2141.1990.tb07892.x

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Article

Homozygous deletion of FMS in a patient with the 5q- syndrome.

British journal of haematology - 1 Oct 1990

Boultwood J, Rack K, Buckle V J, Kelly S, Madden J, Oscier D G, Wainscoat J S

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 2094336
DOI: 10.1111/j.1365-2141.1990.tb07892.x

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 8 closest

Homozygous deletion of FMS in a patient with the 5q- syndrome.PMID 2094336Read ↗

A de novo deletion in FMR1 in a patient with developmental delay.Semantic proximity Read ↗

Terminal deletion of chromosome 5p in a patient with phenotypical features of Lujan-Fryns syndrome.Semantic proximity Read ↗

5p deletions: Current knowledge and future directions.Semantic proximity Read ↗

An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype.Semantic proximity Read ↗

Syndromic congenital myelofibrosis associated with a loss-of-function variant in RBSN.Semantic proximity Read ↗

A case of Netherton syndrome with mutation in SPINK5 and FLG.Semantic proximity Read ↗

Fragile X syndrome phenotype with normal FMR1 gene studies.Semantic proximity Read ↗

Identification of a De Novo Heterozygous Frameshift Variant in FMR1 in a Female With Fragile X Syndrome.Semantic proximity Read ↗

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