Literature DB >> 16760743

Ser351Cys mutation in the fibroblast growth factor receptor 2 gene results in severe Pfeiffer syndrome.

Cathy A Stevens1, Elizabeth R Roeder.   

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Year:  2006        PMID： 16760743     DOI： 10.1097/01.mcd.0000198930.32200.73

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  3 in total

1.  Exclusion of Class III malocclusion candidate loci in Brazilian families.

Authors:  R M Cruz; J K Hartsfield; G Falcão-Alencar; D L Koller; R W Pereira; J Mah; I Ferrari; S F Oliveira
Journal:  J Dent Res       Date:  2011-08-01       Impact factor: 6.116

Review 2.  Understanding craniosynostosis as a growth disorder.

Authors:  Kevin Flaherty; Nandini Singh; Joan T Richtsmeier
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2016-03-22       Impact factor: 5.814

3.  Pfeiffer syndrome in an adult with previous surgical correction: A case report of CT findings.

Authors:  Neil Duggal; Adil Omer; Sandhya Jupalli; Leszek Pisinski; Alan V Krauthamer
Journal:  Radiol Case Rep       Date:  2021-07-02
  3 in total

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