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Quoted phrase not found in phrase index: "Auriculocondylar syndrome 1"
Page 1
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.
Rieder MJ, Green GE, Park SS, Stamper BD, Gordon CT, Johnson JM, Cunniff CM, Smith JD, Emery SB, Lyonnet S, Amiel J, Holder M, Heggie AA, Bamshad MJ, Nickerson DA, Cox TC, Hing AV, Horst JA, Cunningham ML. Rieder MJ, et al. Am J Hum Genet. 2012 May 4;90(5):907-14. doi: 10.1016/j.ajhg.2012.04.002. Am J Hum Genet. 2012. PMID: 22560091 Free PMC article.
Syndromes of the first and second pharyngeal arches: A review.
Passos-Bueno MR, Ornelas CC, Fanganiello RD. Passos-Bueno MR, et al. Am J Med Genet A. 2009 Aug;149A(8):1853-9. doi: 10.1002/ajmg.a.32950. Am J Med Genet A. 2009. PMID: 19610085 Review.
Our aim in this review is to discuss currently known mechanisms associated with three important syndromes of the first and second pharyngeal arches: Treacher Collins syndrome (TCS), Oculo-auriculo-vertebral syndrome (AOVS) and Auriculo-Condylar syndrome (ACS) …
Our aim in this review is to discuss currently known mechanisms associated with three important syndromes of the first and second pharyngeal …
Auriculo-condylar syndrome: further evidence for a new disorder.
Guion-Almeida ML, Kokitsu-Nakata NM, Zechi-Ceide RM, Vendramini S. Guion-Almeida ML, et al. Am J Med Genet. 1999 Sep 10;86(2):130-3. doi: 10.1002/(sici)1096-8628(19990910)86:2<130::aid-ajmg8>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10449647