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Article

X-linked lymphoproliferative disease. Detection of a paternally inherited mutation in a German family using haplotype analysis.

American journal of diseases of children (1960) - 1 Dec 1993

Schuster V, Kress W, Friedrich W, Grimm T, Kreth H W

Abstract excerpt

OBJECTIVE: To study the inheritance of the X-linked lymphoproliferative disease (XLP) locus in a German family. DESIGN: Haplotype segregation analysis. SETTING: Departments of Pediatrics and Human Genetics, University of Würzburg and University of Ulm, Federal Republic of Germany. PARTICIPANTS: F...

Topics

Base Sequence
Child, Preschool
Female
Genetic Linkage
Genetic Markers
Haplotypes
Humans
Infant
Lymphoproliferative Disorders
Male
Molecular Sequence Data
Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Pedigree

X Chromosome

Source

Identifiers

PMID: 8249949
DOI: 10.1001/archpedi.1993.02160360045015

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8249949-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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