سندرم ای‌ای‌سی (Persian Wikipedia)

Analysis of information sources in references of the Wikipedia article "سندرم ای‌ای‌سی" in Persian language version.

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archive.org

Peterson-Falzone, Sally J.; Mary A. Hardin-Jones; Michael P. Karnell; Betty Jane McWilliams (2001). Cleft Palate Speech. Mosby. ISBN 978-0-8151-3153-3.
Shprintzen, Robert J. (1997). Genetics, Syndromes, and Communication Disorders. Singular Pub. Group. ISBN 978-1-56593-620-1.

Buss PW, Hughes HE, Clarke A (September 1995). "Twenty-four cases of the EEC syndrome: clinical presentation and management". Journal of Medical Genetics. 32 (9): 716–723. doi:10.1136/jmg.32.9.716. PMC 1051673. PMID 8544192.
Celli J, Duijf P, Hamel BC, et al. (1999). "Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome". Cell. 99 (2): 143–153. doi:10.1016/S0092-8674(00)81646-3. PMID 10535733.
Ramirez D, Lammer EJ (2004). "Lacrimoauriculodentodigital syndrome with cleft lip/palate and renal manifestations". Cleft Palate Craniofacial Journal. 41 (5): 501–506. doi:10.1597/03-080.1. PMID 15352854.
Brunner HG, Hamel BC, Van Bokhoven H (2002). "The p63 gene in EEC and other syndromes". Journal of Medical Genetics. 39 (6): 377–381. doi:10.1136/jmg.39.6.377. PMC 1735150. PMID 12070241.

Buss PW, Hughes HE, Clarke A (September 1995). "Twenty-four cases of the EEC syndrome: clinical presentation and management". Journal of Medical Genetics. 32 (9): 716–723. doi:10.1136/jmg.32.9.716. PMC 1051673. PMID 8544192.
Celli J, Duijf P, Hamel BC, et al. (1999). "Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome". Cell. 99 (2): 143–153. doi:10.1016/S0092-8674(00)81646-3. PMID 10535733.
Ramirez D, Lammer EJ (2004). "Lacrimoauriculodentodigital syndrome with cleft lip/palate and renal manifestations". Cleft Palate Craniofacial Journal. 41 (5): 501–506. doi:10.1597/03-080.1. PMID 15352854.
Brunner HG, Hamel BC, Van Bokhoven H (2002). "The p63 gene in EEC and other syndromes". Journal of Medical Genetics. 39 (6): 377–381. doi:10.1136/jmg.39.6.377. PMC 1735150. PMID 12070241.