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Article

Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype.

Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas - 1 Aug 2008

Rodríguez V R, Mazzucato L F, Pina-Neto J M

Abstract excerpt

Monosomy 1p36 is the most common subtelomeric microdeletion syndrome with an incidence rate estimated to be 1 in 5000 births. A hypothesis of a similarity between patients with 1p36 deletion and those with Prader-Willi syndrome and the existence of two different phenotypes for 1p36 microdeletion...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18797701
DOI: 10.1590/s0100-879x2008000800007

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18797701-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype.PMID 18797701Read ↗

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Population data suggest that deletions of 1p36 are a relatively common chromosome abnormalitySemantic proximity Read ↗

Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype.Semantic proximity Read ↗

Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia.Semantic proximity Read ↗

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Investigating the correlation between genotype and phenotype in Prader-Willi syndrome: a study of 45 cases from Brazil.Semantic proximity Read ↗

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Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalities.Semantic proximity Read ↗

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