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1 ere limited to a 3% excess rate of a bulging fontanelle.
2 natal vitamin A supplementation or a bulging fontanelle.
3 ive index during compression of the anterior fontanelle.
4 dult sheep skull to model the human anterior fontanelle.
5 , with minima at the nasion and the anterior fontanelle.
6 r (8.5-MHz probe) and mastoid (13-MHz probe) fontanelles.
7 a, flat midface, receding forehead, and wide fontanelles.
8 his deletion syndrome include large anterior fontanelle (100%), motor delay/hypotonia (92%), moderate
9 53 infants were reported to have a bulging fontanelle; 32 (0.3%) in the vitamin A group and 21 (0.2
11 lle (n = 91) and 432 children who had normal fontanelles after receiving vitamin A or placebo were ev
12 re, absence of hyoid bone, failed closure of fontanelle, bifid xiphoid process and hypoplasia of clav
18 ed by hypoplastic or absent clavicles, large fontanelles, dental anomalies and delayed skeletal devel
19 stence of a metopic suture and open anterior fontanelle early in hominin evolution, and they put an e
20 fossil record do not support the metopic and fontanelle features proposed by Falk and colleagues.
21 ll triangular-shaped remnant of the anterior fontanelle, from which a clear metopic suture (MS) cours
22 esulted in clavicular hypoplasia and delayed fontanelle fusion, a phenotype similar to the cleidocran
23 sion models predicting each score, a bulging fontanelle had a small negative effect in all models; wh
24 aging to measure oxygen saturation through a fontanelle has been demonstrated in large animals in-viv
25 n the placebo group, children with a bulging fontanelle in the vitamin A group tended to grow less (-
27 0.5 cm, P = 0.33), whereas those with normal fontanelles in the vitamin A group grew significantly mo
30 ed from the analysis the effect of a bulging fontanelle was not significant in any model (P > or = 0.
31 ransient fibrous joints known as sutures and fontanelles, which are essential for skull compression d