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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 has been suggested. The main objective of the present study was to determine the existence of 1p36 microdeletion in a...

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Source

Identifiers

PMID: 18797701
DOI: 10.1590/s0100-879x2008000800007

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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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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 ↗

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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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