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

Identification of an autosomal recessive mode of inheritance in paediatric Behçet's families by segregation analysis.

American journal of medical genetics. Part A - 1 Oct 2003

Molinari N, Koné Paut I, Manna R, Demaille J, Daures J P, Touitou I

Abstract excerpt

We have conducted a segregation analysis in order to characterise the transmission of Behçet Disease (BD), a multifactorial condition with a strong genetic component. Complete information about BD status and pedigree was obtained on 104 probands from our database. We used the criteria of the Inte...

Read the complete abstract on PubMed

Topics

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

Share to Behcet Syndrome
Share to Data Interpretation, Statistical
Share to Family Health

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Recessive

Share to Genetic Predisposition to Disease

Share to Nuclear Family

Share to Pedigree

Source

Identifiers

PMID: 12955762
DOI: 10.1002/ajmg.a.20136

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12955762-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of an autosomal recessive mode of inheritance in paediatric Behçet's families by segregation analysis.PMID 12955762Read ↗

Cluster analysis of paediatric Behçet's disease: Data from The Pediatric Rheumatology Academy-Research Group.Semantic proximity Read ↗

Behçet's disease: familial clustering and immunogenetics.Semantic proximity Read ↗

Familial Behçet's disease.Semantic proximity Read ↗

Age-related differences in the clinical phenotypes of Behçet's disease: The experience of two referral centres.Semantic proximity Read ↗

Segregation analysis of quantitative traits.Semantic proximity Read ↗

Genetic anticipation in Behçet's syndrome.Semantic proximity Read ↗

Segregation analysis of microcephaly.Semantic proximity Read ↗

Segregation analysis in Shwachman-Diamond syndrome: evidence for recessive inheritance.Semantic proximity Read ↗

Segregation analysis of autosomal dominant polycystic kidney disease.Semantic proximity Read ↗

Segregation analysis of Scheuermann disease in ninety families from Siberia.Semantic proximity Read ↗

MICA gene polymorphisms in an Italian paediatric series of juvenile Behçet disease.Semantic proximity Read ↗

Segregation analysis of Alagille syndrome.Semantic proximity Read ↗

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