Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Retroviral gene transfer for the assignment of Fanconi anemia (FA) patients to a FA complementation group.

Human genetics - 1 Feb 1998

Fu K L, Thuss P C, Fujino T, Digweed M, Liu J M, Walsh C E

Abstract excerpt

Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, cancer susceptibility, and a variety of developmental defects. The disease is clinically heterogeneous; eight different complementation groups (FA A-H) and, thus, genetic loci have been discovered. Two ge...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cell Cycle
Share to Cell Line
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to DNA-Binding Proteins

Share to Fibroblasts

Share to Genetic Complementation Test

Share to Lymphocyte Activation

Source

Identifiers

PMID: 9521584
DOI: 10.1007/s004390050671

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-9521584-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Retroviral gene transfer for the assignment of Fanconi anemia (FA) patients to a FA complementation group.PMID 9521584Read ↗

A rapid method for retrovirus-mediated identification of complementation groups in Fanconi anemia patients.Semantic proximity Read ↗

Functional correction of Fanconi anemia group A hematopoietic cells by retroviral gene transfer.Semantic proximity Read ↗

Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A.Semantic proximity Read ↗

Gene transfer for the eventual treatment of Fanconi's anemia.Semantic proximity Read ↗

Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.Semantic proximity Read ↗

Positional cloning of the Fanconi anaemia group A gene.Semantic proximity Read ↗

Cloning of cDNAs for Fanconi's anaemia by functional complementation.Semantic proximity Read ↗

Phenotypic correction of Fanconi anemia in human hematopoietic cells with a recombinant adeno-associated virus vector.Semantic proximity Read ↗

Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.Semantic proximity Read ↗

Validation of Fanconi anemia complementation Group A assignment using molecular analysis.Semantic proximity Read ↗

A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network.Semantic proximity Read ↗

Functional analysis of patient-derived mutations in the Fanconi anemia gene, FANCG/XRCC9.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.