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Article

Apert syndrome.

Journal of the Indian Medical Association - 1 Apr 1996

Deshmukh L S, Rasheed S M

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PMID: 8854639

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Related research

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Apert Syndrome with Preaxial Polydactyly with FGFR2 Gene Mutation.Semantic proximity Read ↗

Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene?Semantic proximity Read ↗

Understanding the molecular basis of Apert syndrome.Semantic proximity Read ↗

[Apert syndrome or acrocephalosyndactilia type I].Semantic proximity Read ↗

Atypical presentation of a newborn with Apert syndrome.Semantic proximity Read ↗

Apert syndrome: evaluation of a treatment algorithm.Semantic proximity Read ↗

Alport syndrome--clinical phenotypes, incidence, and pathology.Semantic proximity Read ↗

Uncoupling fibroblast growth factor receptor 2 ligand binding specificity leads to Apert syndrome-like phenotypes.Semantic proximity Read ↗

Apert syndrome with omphalocele: a case report.Semantic proximity Read ↗

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