Corona-Rivera A - Search Results

1

Characterization of two ectrodactyly-associated translocation breakpoints separated by 2.5 Mb on chromosome 2q14.1-q14.2.

David D, Marques B, Ferreira C, Vieira P, Corona-Rivera A, Ferreira JC, van Bokhoven H. David D, et al. Eur J Hum Genet. 2009 Aug;17(8):1024-33. doi: 10.1038/ejhg.2009.2. Epub 2009 Feb 18. Eur J Hum Genet. 2009. PMID: 19223936 Free PMC article.

2

Ring chromosome 6 in a child with anterior segment dysgenesis and review of its overlap with other FOXC1 deletion phenotypes.

Corona-Rivera JR, Corona-Rivera A, Zepeda-Romero LC, Rios-Flores IM, Rivera-Vargas J, Orozco-Vela M, Santana-Bejarano UF, Torres-Anguiano E, Pinto-Cardoso M, David D, Bobadilla-Morales L. Corona-Rivera JR, et al. Congenit Anom (Kyoto). 2019 Sep;59(5):174-178. doi: 10.1111/cga.12309. Epub 2018 Oct 9. Congenit Anom (Kyoto). 2019. PMID: 30225942 Review.

3

Holoprosencephaly, hypertelorism, and ectrodactyly in a boy with an apparently balanced de novo t(2;4) (q14.2;q35).

Corona-Rivera A, Corona-Rivera JR, Bobadilla-Morales L, García-Cobian TA, Corona-Rivera E. Corona-Rivera A, et al. Am J Med Genet. 2000 Feb 28;90(5):423-6. doi: 10.1002/(sici)1096-8628(20000228)90:5<423::aid-ajmg12>3.0.co;2-k. Am J Med Genet. 2000. PMID: 10706364

4

Corroboration of the lower extremity counterpart of the Poland sequence.

Corona-Rivera JR, Corona-Rivera A, Totsuka-Sutto SE, Corona-Rivera E. Corona-Rivera JR, et al. Clin Genet. 1997 Apr;51(4):257-9. doi: 10.1111/j.1399-0004.1997.tb02465.x. Clin Genet. 1997. PMID: 9184248

5

Report and review of the fetal brain disruption sequence.

Corona-Rivera JR, Corona-Rivera E, Romero-Velarde E, Hernández-Rocha J, Bobadilla-Morales L, Corona-Rivera A. Corona-Rivera JR, et al. Eur J Pediatr. 2001 Nov;160(11):664-7. doi: 10.1007/s004310100813. Eur J Pediatr. 2001. PMID: 11760023 Review.

6

Cleft lip and/or palate in two cases of 46,X,i(Xq) Turner syndrome.

Corona-Rivera JR, Corona-Rivera E, Bobadilla-Morales L, Garcia-Cobia TA, Corona-Rivera A. Corona-Rivera JR, et al. Genet Couns. 2002;13(1):19-22. Genet Couns. 2002. PMID: 12017233

7

Lumbopedal skin pedicle in an infant with the amniotic band syndrome: a Disorganization-like defect?

Corona-Rivera JR, Corona-Rivera E, Navarro-Ramírez P, Castro-Hernández JF, Acosta-León J, Corona-Rivera A. Corona-Rivera JR, et al. Clin Dysmorphol. 2003 Jan;12(1):51-4. doi: 10.1097/00019605-200301000-00009. Clin Dysmorphol. 2003. PMID: 12514366

8

Chromosome instability induced in vitro with mitomycin C in five Seckel syndrome patients.

Bobabilla-Morales L, Corona-Rivera A, Corona-Rivera JR, Buenrostro C, García-Cobián TA, Corona-Rivera E, Cantú-Garza JM, García-Cruz D. Bobabilla-Morales L, et al. Am J Med Genet A. 2003 Dec 1;123A(2):148-52. doi: 10.1002/ajmg.a.20341. Am J Med Genet A. 2003. PMID: 14598338

9

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.

10

[Occurrence of preterm and term low birth weight deliveries and presence of the Sydney crease].

Corona Rivera JR, Esparza Rodríguez M, Jiménez Leal CM, Corona Rivera A, Pérez Molina Jde J. Corona Rivera JR, et al. Ginecol Obstet Mex. 2005 Jan;73(1):11-8. Ginecol Obstet Mex. 2005. PMID: 15847144 Spanish.

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