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

Polymorphism analysis of Fukuyama type congenital muscular dystrophy (FCMD) siblings with different phenotypes.

Brain & development - 1 Apr 1997

Kondo-Iida E, Saito K, Osawa M, Ishihara T, Toda T, Fukuyama Y

Abstract excerpt

Peak motor function in Fukuyama type congenital muscular dystrophy (FCMD) is generally considered to be no better than sitting without help or sliding on the buttocks. There are a few patients who acquire the ability to stand and a small fraction of our total congenital muscular dystrophy (CMD) population are able to walk at some point. These ambulant cases may reflect a broad spectrum of motor disabilities in...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Alleles
Share to Child

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

Share to Child, Preschool

Share to Genotype

Share to Pedigree

Share to Phenotype

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 9134189
DOI: 10.1016/s0387-7604(96)00556-6

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

Polymorphism analysis of Fukuyama type congenital muscular dystrophy (FCMD) siblings with different phenotypes.PMID 9134189Read ↗

Haplotype-phenotype correlation in Fukuyama congenital muscular dystrophy.Semantic proximity Read ↗

Prenatal diagnosis of Fukuyama-type congenital muscular dystrophy by microsatellite analysis.Semantic proximity Read ↗

Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD).Semantic proximity Read ↗

Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium.Semantic proximity Read ↗

Prenatal diagnosis of Fukuyama type congenital muscular dystrophy by polymorphism analysis.Semantic proximity Read ↗

Analysis of genotype and phenotype in fukuyama congenital muscular dystrophy.Semantic proximity Read ↗

Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.Semantic proximity Read ↗

Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome.Semantic proximity Read ↗

Broader clinical spectrum of Fukuyama-type congenital muscular dystrophy manifested by haplotype analysis.Semantic proximity Read ↗

Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutin.Semantic proximity Read ↗

Seizure-genotype relationship in Fukuyama-type congenital muscular dystrophy.Semantic proximity Read ↗

The mildest known case of Fukuyama-type congenital muscular dystrophy.Semantic proximity Read ↗

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