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Your search for Aurocephalosyndactyly AND humans[mesh] AND review[publication type] retrieved no results
Pfeiffer syndrome.
Vogels A, Fryns JP. Vogels A, et al. Orphanet J Rare Dis. 2006 Jun 1;1:19. doi: 10.1186/1750-1172-1-19. Orphanet J Rare Dis. 2006. PMID: 16740155 Free PMC article. Review.
Nervous system involvement in Pfeiffer syndrome.
Mavridis IN, Rodrigues D. Mavridis IN, et al. Childs Nerv Syst. 2021 Feb;37(2):367-374. doi: 10.1007/s00381-020-04934-7. Epub 2020 Oct 20. Childs Nerv Syst. 2021. PMID: 33083874 Review.
Optic Nerve Atrophy in Syndromic Craniosynostosis.
Fearon JA, Barrientos S, Ditthakasem K, Herbert M. Fearon JA, et al. Plast Reconstr Surg. 2022 Aug 1;150(2):381e-386e. doi: 10.1097/PRS.0000000000009367. Epub 2022 Jun 8. Plast Reconstr Surg. 2022. PMID: 35671456 Review.
Genetic obesity syndromes.
Goldstone AP, Beales PL. Goldstone AP, et al. Front Horm Res. 2008;36:37-60. doi: 10.1159/000115336. Front Horm Res. 2008. PMID: 18230893 Review.
Acrocephalosyndactyly syndromes: a review.
Prevel CD, Eppley BL, McCarty M. Prevel CD, et al. J Craniofac Surg. 1997 Jul;8(4):279-85. doi: 10.1097/00001665-199707000-00010. J Craniofac Surg. 1997. PMID: 9482052 Review.
Over the last quarter century, a revision has taken place in the classification of the acrocephalosyndactyly syndromes. This reflects the advances in molecular biology that have led to improved genetic mapping of these syndromes. In this review we provide an overview of th …
Over the last quarter century, a revision has taken place in the classification of the acrocephalosyndactyly syndromes. This reflects …
Dear old dad.
Glaser RL, Jabs EW. Glaser RL, et al. Sci Aging Knowledge Environ. 2004 Jan 21;2004(3):re1. doi: 10.1126/sageke.2004.3.re1. Sci Aging Knowledge Environ. 2004. PMID: 14736914 Review.
Dental approach for Apert syndrome in children: a systematic review.
López-Estudillo AS, Rosales-Bérber MA, Ruiz-Rodríguez S, Pozos-Guillén A, Noyola-Frías MÁ, Garrocho-Rangel A. López-Estudillo AS, et al. Med Oral Patol Oral Cir Bucal. 2017 Nov 1;22(6):e660-e668. doi: 10.4317/medoral.21628. Med Oral Patol Oral Cir Bucal. 2017. PMID: 29053644 Free PMC article. Review.
BACKGROUND: Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis condition resulting from missense mutations in the gene encoding fibroblast growth factor receptor 2. ...
BACKGROUND: Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis condition resulting from mis …
164 results