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Article

Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene.

American journal of medical genetics. Part A - 1 Aug 2006

Rand Casey M, Weese-Mayer Debra E, Zhou Lili, Maher Brion S, Cooper Margaret E, Marazita Mary L, Berry-Kravis Elizabeth M

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PMID: 16830328
DOI: 10.1002/ajmg.a.31336

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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.

Related research

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Click a neighbor to travelStep 1 · 8 closest

Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene.PMID 16830328Read ↗

Sudden Infant Death Syndrome: Case-Control Frequency Differences at Genes Pertinent to Early Autonomic Nervous System Embryologic DevelopmentSemantic proximity Read ↗

A Common 3′UTR Variant of the PHOX2B Gene Is Associated With Infant Life-Threatening and Sudden Death Events in the Italian PopulationSemantic proximity Read ↗

Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death.Semantic proximity Read ↗

PHOX2B polyalanine repeat length is associated with sudden infant death syndrome and unclassified sudden infant death in the Dutch population.Semantic proximity Read ↗

Causative and common PHOX2B variants define a broad phenotypic spectrumSemantic proximity Read ↗

Sudden infant death syndrome and other causes of infant mortality: diagnosis, mechanisms, and risk for recurrence in siblings.Semantic proximity Read ↗

Genomic risk factors in sudden infant death syndromeSemantic proximity Read ↗

Homeobox genes and human genetic disorders.Semantic proximity Read ↗

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