Camptodactyly, joint contractures, facial, and skeletal defects: Further delineation of the Rozin camptodactyly syndrome by García-Ortiz, J.E., Castañeda-Cisneros, G., López-Cardona, M.G., Sánchez-Corona, J., Patiño-García, B., García-González, C.L., Nazará, Z., Dávalos-Rodríguez, N., Rodríguez, L.X., García-Cruz, D.

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A distinct osteochondrodysplasia with hypertrichosis- Individualization of a probable autosomal recessive entity by Cant, J. M., Garcia-Cruz, D., S nchez-Corona, J., Hern ndez, A., Nazar, Z.

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Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Further delineation of a new genetic syndrome by García-Cruz, D., Sánchez-Corona, J., Nazará, Z., García-Cruz, M. O., Figuera, L. E., Castañeda, V., Cantú, J. M.

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Autosomal dominant acrodysostosis by Cant, J. M., Hern ndez, A., Panduro-Cerda, A., Nazar -Cazorla, Z.

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Prenatal growth retardation, pelvic hypoplasia, and arthrogrypotic changes of lower limbs: A distinct autosomal-recessive disorder by Sarralde, Augusto, Reynoso, Martha C., Nazará, Zamira, Soto, Fernando, Hernández, Alejandro

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A probably distinct autosomal recessive thoraco-limb dysplasia by Rivera, H, Perez-Salas, J M, Nazara, Z, Ramirez, M L

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Camptodactyly, joint contractures, facial, and skeletal defects: Further delineation of the Rozin camptodactyly syndrome by García-Ortiz, J E, Castañeda-Cisneros, G, López-Cardona, M G, Sánchez-Corona, J, Patiño-García, B, García-González, C L, Nazará, Z, Dávalos-Rodríguez, N, Rodríguez, L X, García-Cruz, D

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Substantial and sustained reduction in under-5 mortality, diarrhea, and pneumonia in Oshikhandass, Pakistan: evidence from two longitudinal cohort studies 15 years apart by Hansen, C L, McCormick, B J J, Azam, S I, Ahmed, K, Baker, J M, Hussain, E, Jahan, A, Jamison, A F, Knobler, S L, Samji, N, Shah, W H, Spiro, D J, Thomas, E D, Viboud, C, Rasmussen, Z A

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