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APERTPersonnel Turnover Percentage
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References in periodicals archive ?
Hagberg, "Dental agenesis patterns of permanent teeth in Apert syndrome," European Journal of Oral Sciences, vol.
Craniosynostosis syndromes including Apert, Crouzon, Pfeiffer, Jackson-Weiss, and Beare-Stevenson syndromes, and FGFR2-related isolated coronal synostosis occur as a result of FGFR2 gene mutations localized in the 10q25.3-26 locus (2).
(Sekil 1) Bu yontem calismaya dahil edilen Apert sendromlu bir olguda modifiye edildi ve bu hastada sindaktili basparmagin ulnar sinirindan yapilan lineer bir insizyonla acildi (Sekil 2).
We have reported a rare congenital malformation Apert syndrome or achrocephalosyndactyly.
24-year-old Johnny Reay from Stoneleigh was born with Apert's Syndrome, a genetic condition leading to 1 in 66 thousand children born with their fingers and toes fused together.
Error Beta 1 (Constant) -41.685 7.922 -5.262 Log_PIBpc 4.536 1.220 .331 3.719 Cons .342 .061 .475 5.571 1 Topi -.451 .127 -.236 -3.561 Top 10 .150 .057 .195 2.627 Apert .024 .008 .210 3.080 Infl .005 .084 .004 .057 Escol -.080 .028 -.206 -2.858 Model B Sig.
Apert Syndrome is a condition that prevents the skull from growing correctly, and it has a profound effect on the shape of the individual's face and head.
Multiple coalitions can be associated with syndromes, such as Apert syndrome, or disorders such as fibular hemimelia.