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Article

A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255.

Journal of medical genetics - 1 Sept 1995

Bennett C P, Barnicoat A J, Cotter F, Wang Q, Mathew C G

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 8544203
DOI: 10.1136/jmg.32.9.757
PMCID: PMC1051687

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255.PMID 8544203Read ↗

Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease gene.Semantic proximity Read ↗

A gain-of-function variant in the Wiskott-Aldrich syndrome gene is associated with a MYH9-related disease-like syndrome.Semantic proximity Read ↗

Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.Semantic proximity Read ↗

Mutation watch: PEX PLUS? Gene(s) for X-linked hypophosphatemia and deafness.Semantic proximity Read ↗

X-linked Wiskott-Aldrich syndrome in a girl.Semantic proximity Read ↗

Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134.Semantic proximity Read ↗

Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease.Semantic proximity Read ↗

Scanning of the Wiskott-Aldrich syndrome (WAS) gene: identification of 18 novel alterations including a possible mutation hotspot at Arg86 resulting in thrombocytopenia, a mild WAS phenotype.Semantic proximity Read ↗

Fragile X syndrome and other dynamic mutation diseases.Semantic proximity Read ↗

Two 3' polymorphisms in DLX5: g126427delTATC and g126249T-->C.Semantic proximity Read ↗

WT1 nephropathy in a girl with normal karyotype (46,XX)Semantic proximity Read ↗

Phenotypic Findings in Patients With KCNJ2-Related Anderson-Tawil Syndrome.Semantic proximity Read ↗

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