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Article

No correlation between phenotype and genotype in boys with a truncating MECP2 mutation.

Journal of medical genetics - 1 Jan 2003

Ravn K, Nielsen J B, Uldall P, Hansen F J, Schwartz M

Abstract excerpt

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

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Source

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Identifiers

PMID: 12525553
DOI: 10.1136/jmg.40.1.e5
PMCID: PMC1735260

Genes

MECP2

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.

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Semantic proximity does not establish scientific evidence.

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No correlation between phenotype and genotype in boys with a truncating MECP2 mutation.PMID 12525553Read ↗

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MECP2 Dysautonomia Phenotypes in Boys.Semantic proximity Read ↗

Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort studySemantic proximity Read ↗

Meckel–Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in EuropeSemantic proximity Read ↗

[Nervous and mental diseases in boys and mutations in MECP2 gene].Semantic proximity Read ↗

Clinical utility gene card for: Meckel syndrome - update 2016.Semantic proximity Read ↗

De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to ThriveSemantic proximity Read ↗

MECP2-Related Disorders in Males.Semantic proximity Read ↗

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