Corona-Rivera E - Search Results

1

De novo partial trisomy of chromosome 18(pter yields q11:). Some observations on the phenotype mapping of chromosome 18 imbalances.

Hernandez A, Corona-Rivera E, Plascencia L, Nazara Z, Ibarra B, Cantu JM. Hernandez A, et al. Ann Genet. 1979;22(3):165-7. Ann Genet. 1979. PMID: 316674

2

Further clinical and radiological features in metaphyseal chondrodysplasia Jansen type.

Nazará Z, Hernández A, Corona-Rivera E, Vaca G, Panduro A, Martínez-Basalo C, Cantú JM. Nazará Z, et al. Radiology. 1981 Sep;140(3):697-700. doi: 10.1148/radiology.140.3.6974367. Radiology. 1981. PMID: 6974367

3

[Clinical and genetic aspects of cherubism (author's transl)].

Corona-Rivera E, Padilla HM, Garzón-de-la-Mora M, Delgado ML, Zavala C, Nazará-Cazorla Z, Hernández A, Cantú JM. Corona-Rivera E, et al. Schweiz Rundsch Med Prax. 1980 Nov 18;69(46):1683-8. Schweiz Rundsch Med Prax. 1980. PMID: 7267594 French. No abstract available.

4

[Prenatal factors and congenital defects in 7,791 consecutive births].

Hernández A, Corona-Rivera E, Martínez-Basalo C, Aguirre-Negrete G, Fonseca S, Cantú JM. Hernández A, et al. Bol Med Hosp Infant Mex. 1983 Jul;40(7):363-6. Bol Med Hosp Infant Mex. 1983. PMID: 6684938 Spanish. No abstract available.

5

[Holt syndrome: an autosomal dominant, heterogeneous, acral malformation].

Hernández Téllez A, Corona Rivera E, Martínez-Basalo C, Nazará Cazorla Z, Aguirre-Negrete MG, Cantú JM. Hernández Téllez A, et al. Bol Med Hosp Infant Mex. 1982 Feb;39(2):131-3. Bol Med Hosp Infant Mex. 1982. PMID: 7093017 Spanish. No abstract available.

6

Post-pubertal female psychosexual orientation in incomplete male pseudohermaphroditism type 2 (5 alpha-reductase deficiency).

Cantú JM, Corona-Rivera E, Díaz M, Medina C, Esquinca E, Cortés-Gallegos V, Vaca G, Hernández A. Cantú JM, et al. Acta Endocrinol (Copenh). 1980 Jun;94(2):273-9. doi: 10.1530/acta.0.0940273. Acta Endocrinol (Copenh). 1980. PMID: 6774548

7

The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidism.

Martínez y Martínez R, Ocampo-Campos R, Pérez-Arroyo R, Corona-Rivera E, Cantú JM. Martínez y Martínez R, et al. Eur J Pediatr. 1985 Jan;143(3):233-5. doi: 10.1007/BF00442150. Eur J Pediatr. 1985. PMID: 3987723

8

A new probably autosomal recessive cardiomelic dysplasia with mesoaxial hexadactyly.

Martínez y Martínez R, Corona-Rivera E, Jiménez-Martínez M, Ocampo-Campos R, García-Maravilla S, Cantú JM. Martínez y Martínez R, et al. J Med Genet. 1981 Apr;18(2):151-4. doi: 10.1136/jmg.18.2.151. J Med Genet. 1981. PMID: 7241534 Free PMC article.

9

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. Among authors: corona rivera e. 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

10

Infant with manifestations of oto-palato-digital syndrome type II and of Melnick-Needles syndrome.

Corona-Rivera JR, Corona-Rivera E, Corona-Rivera A, Quiles-Corona M, Velez-Gómez E, Arana-Gutiérrez MA. Corona-Rivera JR, et al. Among authors: corona rivera e. Am J Med Genet. 1999 Jul 2;85(1):79-81. doi: 10.1002/(sici)1096-8628(19990702)85:1<79::aid-ajmg13>3.0.co;2-n. Am J Med Genet. 1999. PMID: 10377016 No abstract available.

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