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

Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.

American journal of medical genetics - 1 Mar 1993

Charrow J, Listernick R, Ward K

Abstract excerpt

Multiple café-au-lait spots have been observed in successive generations of several families without any other manifestations of neurofibromatosis (NF) or any other systemic disorder. The café-au-lait spots in these families segregate as an autosomal dominant trait. The relationship (if any) between the gene for this trait and the NF-1 gene has previously been unknown. We describe a family with five individuals...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Genes, Dominant
Share to Genetic Linkage

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Haplotypes

Share to Infant

Share to Neurofibromatosis 1

Share to Pedigree

Source

Identifiers

PMID: 8456833
DOI: 10.1002/ajmg.1320450518

Provenance

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

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.PMID 8456833Read ↗

Familial café au lait spots: a variant of neurofibromatosis type 1.Semantic proximity Read ↗

A severe form of Noonan syndrome and autosomal dominant café-au-lait spots - evidence for different genetic origins.Semantic proximity Read ↗

Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spots.Semantic proximity Read ↗

Giant café-au-lait macule in neurofibromatosis 1: a type 2 segmental manifestation of neurofibromatosis 1?Semantic proximity Read ↗

Cafe au Lait Spots: The Pediatrician's PerspectiveSemantic proximity Read ↗

Multiple café au lait spots in familial patients with MAP2K2 mutation.Semantic proximity Read ↗

Legius Syndrome and its Relationship with Neurofibromatosis Type 1.Semantic proximity Read ↗

Multiple or familial café-au-lait spots is neurofibromatosis type 6: clarification of a diagnosis.Semantic proximity Read ↗

Predicting neurofibromatosis type 1 risk among children with isolated café-au-lait macules.Semantic proximity Read ↗

Analysis of intrafamilial phenotypic variation in neurofibromatosis 1 (NF1).Semantic proximity Read ↗

Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene.Semantic proximity Read ↗

Café-au-lait macules and intertriginous freckling in piebaldism: clinical overlap with neurofibromatosis type 1 and Legius syndrome.Semantic proximity Read ↗

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