Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex
Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex
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Publisher
Switzerland: MDPI AG
Journal title
Language
English
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Publisher
Switzerland: MDPI AG
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Scope and Contents
Contents
The phenotype currently accepted as Pierre Robin syndrome/sequence/anomalad/complex (PR) is characterized by mandibular dysmorphology, glossoptosis, respiratory obstruction, and in some cases, cleft palate. A causative sequence of developmental events is hypothesized for PR, but few clear causal relationships between discovered genetic variants, dy...
Alternative Titles
Full title
Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex
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TN_cdi_doaj_primary_oai_doaj_org_article_4ae91ca537a148c1ab2b2ba30532a896
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_4ae91ca537a148c1ab2b2ba30532a896
Other Identifiers
ISSN
2221-3759
E-ISSN
2221-3759
DOI
10.3390/jdb8040030
