Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathy von Peña‐Padilla, C., Marshall, C.R., Walker, S., Scherer, S.W., Tavares‐Macías, G., Razo‐Jiménez, G., Bobadilla‐Morales, L., Acosta‐Fernández, E., Corona‐Rivera, A., Mendoza‐Londono, R., Corona‐Rivera, J. R.

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Risk of alterations in neurodevelopment in infants and preschool children with cancer von Velasco-Hidalgo, Liliana, González-Garay, Alejandro, Rizzoli-Córdoba, Antonio, Rivera-Luna, Roberto, García-Guzmán, Alda, Ortiz-Razo, Ana G., Olmedo-Jiménez, Evereth A., Cárdenas-Cardos, Rocío, Carmona-Jaimez, Kenya S., Zapata-Tarrés, Marta M.

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Impact of Fluoride Exposure on Rat Placenta: Foetal/Placental Morphometric Alterations and Decreased Placental Vascular Density von Guerrero-Arroyo, Jonathan, Jiménez-Córdova, Mónica I., Aztatzi-Aguilar, Octavio G., Del Razo, Luz M.

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Niveles de plomo en sangre conservada en bancos de sangre para transfundir a pacientes pediátricos hospitalizados von Rangel-Calvillo, Martín Noé, del Razo-Jiménez, Luz M., González-González, Patricia

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Childhood lead poisoning from the smelter in Torreón, México von Soto-Jiménez, Martin F., Flegal, Arthur R.

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Intraflagellar transporter protein 140 (IFT140), a component of IFT‐A complex, is essential for male fertility and spermiogenesis in mice von Zhang, Yong, Liu, Hong, Li, Wei, Zhang, Zhengang, Zhang, Shiyang, Teves, Maria E, Stevens, Courtney, Foster, James A, Campbell, Gregory E, Windle, Jolene J, Hess, Rex A, Pazour, Gregory J, Zhang, Zhibing

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Whole genome sequencing in the diagnosis of primary ciliary dyskinesia von Wheway, Gabrielle, Thomas, N Simon, Carroll, Mary, Coles, Janice, Doherty, Regan, Goggin, Patricia, Green, Ben, Harris, Amanda, Hunt, David, Jackson, Claire L, Lord, Jenny, Mennella, Vito, Thompson, James, Walker, Woolf T, Lucas, Jane S

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The Role of IFT140 in Osteogenesis of Adult Mice Long Bone von Tao, Dike, Xue, Hui, Zhang, Chenyang, Li, Gongchen, Sun, Yao

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Acknowledgment to the Reviewers of Metabolites in 2022 von Office, Metabolites Editorial

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Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome von Helm, Benjamin M, Willer, Jason R, Sadeghpour, Azita, Golzio, Christelle, Crouch, Eric, Vergano, Samantha Schrier, Katsanis, Nicholas, Davis, Erica E

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Teratogenic effect on bone tissue development in Rattus norvegicus Wistar strain, induced by the presence of arsenic von Quiterio-Pérez, Mireya, Gaytán-Oyarzún, Juan Carlos, Gordillo-Martínez, Alberto José, Prieto-García, Francisco

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Acknowledgment to the Reviewers of IMetabolites/I in 2022

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Acknowledgement to Reviewers of IJERPH in 2018

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Construcción y validación de un registro clínico para la atención asistencial de enfermería von López-Cocotle, J.J., Moreno-Monsiváis, M.G., Saavedra-Vélez, C.H.

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