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Article

PRRX1 is mutated in a fetus with agnathia-otocephaly.

Clinical genetics - 1 Mar 2011

Sergi C, Kamnasaran D

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Share to Abnormalities, Multiple
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Share to Fetal Death

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

Share to Gene Expression Regulation, Developmental

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Source

Identifiers

PMID: 21294718
DOI: 10.1111/j.1399-0004.2010.01531.x

Genes

PRRX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 19 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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PRRX1 is mutated in a fetus with agnathia-otocephaly.PMID 21294718Read ↗

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Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome.Semantic proximity Read ↗

Expanding the spectrum of SMAD3-related phenotypes to agnathia-otocephaly.Semantic proximity Read ↗

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