Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Muenke Syndrome[original query] |
---|
Clinical and molecular diagnosis of the skeletal dysplasias associated with mutations in the gene encoding Fibroblast Growth Factor Receptor 3 (FGFR3) in Portugal. Clinical genetics 2009 Feb 75 (2): 150-6. Almeida M R, Campos-Xavier A B, Medeira A, Cordeiro I, Sousa A B, Lima M, Soares G, Rocha M, Saraiva J, Ramos L, Sousa S, Marcelino J P, Correia A, Santos H |
Assessing the midface in Muenke syndrome: A cephalometric analysis and review of the literature. Journal of plastic, reconstructive & aesthetic surgery : JPRAS 2016 Jul . Samra Fares, Bauder Andrew R, Swanson Jordan W, Whitaker Linton A, Bartlett Scott P, Taylor Jesse |
A Pilot Study of Identification Genetic Background of Craniosynostosis Cases. The Journal of craniofacial surgery 2020 11 32 (3): 1059-1062. Atli Emine Ikbal, Yalcintepe Sinem, Atli Engin, Demir Selma, Mail Cisem, Eker Damla, Kalkan Rasime, Gurkan Hak |
- Page last reviewed:Feb 1, 2024
- Content source: