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Jorge Román Corona-Rivera

Servicio de Genética

División de Pediatría

Nuevo Hospital Civil de Guadalajara Dr. Juan I. Menchaca

Hospital-Escuela

Mexico

[email]@cucs.udg.mx

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Servicio de Genética, División de Pediatría, Nuevo Hospital Civil de Guadalajara Dr. Juan I. Menchaca, Hospital-Escuela, Mexico. 2006 - 2010
  • Servicio de Genética, Hospital Civil de Guadalajara Dr. Juan I. Menchaca, and Instituto de Genética Humana Dr. Enrique Corona-Rivera, Centro Universitario de Ciencias de la Salud, Mexico. 2009
  • Dr Enrique Corona-Rivera Institute of Human Genetics, University of Guadalajara Health Sciences Center and Division of Pediatrics, Dr Juan I Menchaca Civil Hospital, Guadalajara, México. 2007
  • Laboratorio de Genética Humana y Clínica de Asesoramiento Génetico, Carrera de Medicina, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Mexico. 2001 - 2005
  • Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Mexico. 2002

References

  1. Holoprosencephaly and genitourinary anomalies in fetal methotrexate syndrome. Corona-Rivera, J.R., Rea-Rosas, A., Santana-Ramírez, A., Acosta-León, J., Hernández-Rocha, J., Miguel-Jiménez, K. Am. J. Med. Genet. A (2010) [Pubmed]
  2. Abnormal oral-pharyngeal swallowing as cause of morbidity and early death in Stüve-Wiedemann syndrome. Corona-Rivera, J.R., Cormier-Daire, V., Dagoneau, N., Coello-Ramírez, P., López-Marure, E., Romo-Huerta, C.O., Silva-Baez, H., Aguirre-Salas, L.M., Estrada-Solorio, M.I. Eur. J. Med. Genet (2009) [Pubmed]
  3. Umbilical cord disruption sequence caused by long cord in two unrelated infants with amyoplasia. Corona-Rivera, J.R., García-Cruz, D., Estrada-Padilla, S.A., Pérez-Molina, J.J., Villafuerte-Bautista, M.A., Tavares-Macías, G., Cárdenas-Ruíz-Velasco, J.J. Fetal. Pediatr. Pathol (2009) [Pubmed]
  4. Further clinical delineation of Fine-Lubinsky syndrome. Corona-Rivera, J.R., López-Marure, E., García-Cruz, D., Romo-Huerta, C.O., Rea-Rosas, A., Orozco-Alatorre, L.G., Ramírez-Valdivia, J.M. Am. J. Med. Genet. A (2009) [Pubmed]
  5. Airway anomalies in the oculoauriculofrontonasal syndrome. Román Corona-Rivera, J., López-Marure, E., Gómez-Ruíz, L., del Carmen Abreu-Fernández, M., Quezada-López, C., Pérez-Molina, J., Santibañez-Escobar, L.P. Clin. Dysmorphol. (2007) [Pubmed]
  6. Sydney crease frequency changes among the newborns and infants. Corona-Rivera, J.R., Zarate-Ramírez, S., Pérez-Molina, J.J., Corona-Rivera, A. Am. J. Med. Genet. A (2007) [Pubmed]
  7. Hepatoblastoma in a patient with Goldenhar syndrome born to a diabetic mother. Corona-Rivera, J.R., Sánchez-Zubieta, F., Silva-Padilla, N., González-Ramella, O., López-Marure, E., Vélez-Gómez, E., Orozco-Pérez, J., Soto-Chávez, V., Corona-Rivera, A. Am. J. Med. Genet. A (2006) [Pubmed]
  8. Mental retardation in a boy with anterior cervical hypertrichosis. Corona-Rivera, J.R., González-Abarca, S., Hernández-Rocha, J., García-Cruz, D., Corona-Rivera, A. Am. J. Med. Genet. A (2005) [Pubmed]
  9. Probable new syndrome in a Mexican family with congenital palmar polyonychia and postaxial limb defects. Román Corona-Rivera, J., Corona-Rivera, E., Fragoso-Herrera, R., Nuño-Arana, I., Loera-Castañeda, V. Am. J. Med. Genet. A (2004) [Pubmed]
  10. Lumbopedal skin pedicle in an infant with the amniotic band syndrome: a Disorganization-like defect?. Corona-Rivera, J.R., Corona-Rivera, E., Navarro-Ramírez, P., Castro-Hernández, J.F., Acosta-León, J., Corona-Rivera, A. Clin. Dysmorphol. (2003) [Pubmed]
  11. Cleft lip and/or palate in two cases of 46,X,i(Xq) Turner syndrome. Corona-Rivera, J.R., Corona-Rivera, E., Bobadilla-Morales, L., Garcia-Cobia, T.A., Corona-Rivera, A. Genet. Couns. (2002) [Pubmed]
  12. Report and review of the fetal brain disruption sequence. Corona-Rivera, J.R., Corona-Rivera, E., Romero-Velarde, E., Hernández-Rocha, J., Bobadilla-Morales, L., Corona-Rivera, A. Eur. J. Pediatr. (2001) [Pubmed]
 
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