Analysis of Genetic Factors in a Family With Short Stature. [PDF]
We identified pathogenic variants of two different genes, COL1A2 and GH1, in a family with short stature through trio‐WES, thereby providing a clear genetic diagnosis for this family. ABSTRACT Background To elucidate the genetic underpinnings of short stature in a familial cohort of five individuals.
Zhang S, Zuo T, Deng Y, Zhao D, Liao L.
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Wnt/β-Catenin Pathway and Hydraulic Calcium Silicate-Based Cements: A Narrative Review. [PDF]
Del Giudice C +6 more
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Functional and Aesthetic Treatment of Patients With Tooth Structure Anomalies: A Narrative Review. [PDF]
Reuter AK, Ehlers V.
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Phenotypic spectrum and quality of life in pediatric Bruck syndrome due to FKBP10 and PLOD2 variants: a 2-center United Arab Emirates experience. [PDF]
Awad MH +10 more
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Efficacy of theracal as pulp capping material in permanent dentition: a systematic review and meta-analysis. [PDF]
Mohamed MA +6 more
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Effects of dentinogenesis imperfecta, sex, and tooth type on the compositional and structural organization of the dentin-enamel junction in the osteogenesis imperfecta murine model. [PDF]
Katebifar S +4 more
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Beyond the diagnosis: Unraveling <i>DSPP</i> genotype-phenotype correlations in dentin dysplasia and dentinogenesis imperfecta. [PDF]
Boonyakanog A +8 more
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Management of an Oblique Cervical Root Fracture in an Immature Maxillary Central Incisor: A Case Report. [PDF]
Kodonas K, Fardi A.
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Splicing mutation in DSPP causes dentinogenesis imperfecta and amelogenesis imperfecta. [PDF]
Zhang Z +7 more
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Special Issue "Research in iPSC-Based Disease Models". [PDF]
Deneault E.
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