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Page 1
Further clinical delineation of Fine-Lubinsky syndrome.
Corona-Rivera JR, López-Marure E, García-Cruz D, Romo-Huerta CO, Rea-Rosas A, Orozco-Alatorre LG, Ramírez-Valdivia JM. Corona-Rivera JR, et al. Am J Med Genet A. 2009 May;149A(5):1070-5. doi: 10.1002/ajmg.a.32780. Am J Med Genet A. 2009. PMID: 19396831 Review. No abstract available.
Mental retardation in a boy with anterior cervical hypertrichosis.
Corona-Rivera JR, González-Abarca S, Hernández-Rocha J, García-Cruz D, Corona-Rivera A. Corona-Rivera JR, et al. Am J Med Genet A. 2005 May 15;135(1):69-71. doi: 10.1002/ajmg.a.30669. Am J Med Genet A. 2005. PMID: 15800907 Review.
[Anterior cervical hypertrichosis: case report].
Orozco-Gutiérrez MH, Sánchez-Corona J, García-Ortiz JE, Castañeda-Cisneros G, Dávalos-Rodríguez NO, Corona-Rivera JR, García-Cruz D. Orozco-Gutiérrez MH, et al. Arch Argent Pediatr. 2016 Oct 1;114(5):e314-8. doi: 10.5546/aap.2016.e314. Epub 2016 Oct 1. Arch Argent Pediatr. 2016. PMID: 27606653 Free article. Spanish.
Prevalence of orofacial clefts and risks for nonsyndromic cleft lip with or without cleft palate in newborns at a university hospital from West Mexico.
Corona-Rivera JR, Bobadilla-Morales L, Corona-Rivera A, Peña-Padilla C, Olvera-Molina S, Orozco-Martín MA, García-Cruz D, Ríos-Flores IM, Gómez-Rodríguez BG, Rivas-Soto G, Pérez-Molina JJ. Corona-Rivera JR, et al. Congenit Anom (Kyoto). 2018 Jul;58(4):117-123. doi: 10.1111/cga.12276. Epub 2018 Mar 4. Congenit Anom (Kyoto). 2018. PMID: 29457660
[New subtype of familial achondrogenesis type IA (Houston-Harris)].
Ramírez-García SA, García-Cruz D, Cervantes-Aragón I, Bitar-Alatorre WE, Dávalos-Rodríguez IP, Dávalos-Rodríguez NO, Corona-Rivera JR, Sánchez-Corona J. Ramírez-García SA, et al. Cir Cir. 2018;86(1):89-98. doi: 10.24875/CIRU.M18000008. Cir Cir. 2018. PMID: 29681641 Spanish.
New subtype of familial achondrogenesis type IA (Houston-Harris).
Ramírez-García SA, García-Cruz D, Cervantes-Aragón I, Bitar-Alatorre WE, Dávalos-Rodríguez IP, Dávalos-Rodríguez NO, Corona-Rivera JR, Sánchez-Corona J. Ramírez-García SA, et al. Cir Cir. 2019;86(1):81-89. doi: 10.24875/CIRUE.M18000013. Cir Cir. 2019. PMID: 30951048 English.
Extracranial midline defects in a patient with craniofrontonasal syndrome with a novel EFNB1 mutation.
Acosta-Fernández E, Zenteno JC, Chacón-Camacho OF, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A, Romo-Huerta CO, Zepeda-Romero LC, López-Marure E, Acosta-León J, García-Cruz D, Maciel-Cruz EJ, Corona-Rivera JR. Acosta-Fernández E, et al. Among authors: garcia cruz d. Am J Med Genet A. 2020 May;182(5):1223-1229. doi: 10.1002/ajmg.a.61506. Epub 2020 Feb 5. Am J Med Genet A. 2020. PMID: 32022998
123 results