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1 Amelx and Mmp20 mutations cause amelogenesis imperfecta.
2 because defects in KLK4 cause hypomaturation amelogenesis imperfecta.
3 human enamelin gene cause autosomal dominant amelogenesis imperfecta.
4 tosomal-recessive hypoplastic-hypomaturation amelogenesis imperfecta.
5 efects have been identified in kindreds with amelogenesis imperfecta.
6 of undiagnosed autosomally dominant cases of amelogenesis imperfecta.
7 enamel are grouped under the classification amelogenesis imperfecta.
8 es the need for family-specific diagnosis of amelogenesis imperfecta.
9 the enamelin gene in kindreds suffering from amelogenesis imperfecta.
10 hreonine, as in some cases of human X-linked amelogenesis imperfecta.
11 ation identified in a case of human X-linked amelogenesis imperfecta.
12 consistent with the diagnosis of hypoplastic amelogenesis imperfecta.
13 ous variants in GPR68 in three families with amelogenesis imperfecta, a genetically and phenotypicall
14 ciated with autosomal-dominant hypocalcified amelogenesis imperfecta (ADHCAI), which is typically cha
22 ge would lead to an enamel defect similar to amelogenesis imperfecta (AI) in humans, we generated tra
23 generalized hypoplastic autosomal-recessive amelogenesis imperfecta (AI) in individuals from six app
33 s the first gene involved in the etiology of amelogenesis imperfecta (AI) that does not encode a secr
34 ively inherited cone-rod dystrophy (CRD) and amelogenesis imperfecta (AI) was first reported by Jalil
35 ort stature with brachyolmia and hypoplastic amelogenesis imperfecta (AI) with almost absent enamel.
36 genes, FAM20A mutations are associated with Amelogenesis Imperfecta (AI) with gingival hyperplasia a
37 ied a family in which pitted hypomineralized amelogenesis imperfecta (AI) with premature enamel failu
38 f26, as a cause of recessive hypomineralized amelogenesis imperfecta (AI), a disease in which the for
39 in gene a prime candidate in the etiology of amelogenesis imperfecta (AI), a genetic disease in which
40 d displayed severe enamel defects that mimic amelogenesis imperfecta (AI), with a rough, irregular en
41 AM gene have been found to cause hypoplastic amelogenesis imperfecta (AI), with phenotypes ranging fr
51 e non-syndromic enamel malformations, termed amelogenesis imperfecta, and ablation of Mmp20 in mice r
53 mutated amelogenin (TgP70T), which leads to amelogenesis imperfecta in humans, have heterogeneous en
55 erized by sensorineural hearing loss (SNHL), amelogenesis imperfecta, nail abnormalities, and occasio
56 hreonine, as in some cases of human X-linked amelogenesis imperfecta or when tyrosyl residues were su
57 hreonine, as in some cases of human X-linked amelogenesis imperfecta or when tyrosyl residues were su
58 c regions similar to those in enamel of male amelogenesis imperfecta patients with an identical mutat
59 in X-linked forms of the human enamel defect amelogenesis imperfecta resulting from amelogenin gene m
60 ions in amelogenin observed in patients with amelogenesis imperfecta who demonstrate defects in ename
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