Frías JL - Search Results

1

Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.

Tamayo ML, Olarte M, Gelvez N, Gómez M, Frías JL, Bernal JE, Florez S, Medina D. Tamayo ML, et al. Among authors: frias jl. Int J Pediatr Otorhinolaryngol. 2009 Jan;73(1):97-101. doi: 10.1016/j.ijporl.2008.10.001. Epub 2008 Nov 21. Int J Pediatr Otorhinolaryngol. 2009. PMID: 19027181

2

Study of the etiology of deafness in an institutionalized population in Colombia.

Tamayo ML, Bernal JE, Tamayo GE, Frias JL. Tamayo ML, et al. Among authors: frias jl. Am J Med Genet. 1992 Nov 1;44(4):405-8. doi: 10.1002/ajmg.1320440403. Am J Med Genet. 1992. PMID: 1442876

3

Usher syndrome: results of a screening program in Colombia.

Tamayo ML, Bernal JE, Tamayo GE, Frias JL, Alvira G, Vergara O, Rodriguez V, Uribe JI, Silva JC. Tamayo ML, et al. Among authors: frias jl. Clin Genet. 1991 Oct;40(4):304-11. doi: 10.1111/j.1399-0004.1991.tb03100.x. Clin Genet. 1991. PMID: 1756603

4

Neuroradiology and clinical aspects of Usher syndrome.

Tamayo ML, Maldonado C, Plaza SL, Alvira GM, Tamayo GE, Zambrano M, Frias JL, Bernal JE. Tamayo ML, et al. Among authors: frias jl. Clin Genet. 1996 Sep;50(3):126-32. doi: 10.1111/j.1399-0004.1996.tb02366.x. Clin Genet. 1996. PMID: 8946110

5

Brain magnetic resonance imaging findings in the Opitz G/BBB syndrome: extension of the spectrum of midline brain anomalies.

MacDonald MR, Schaefer GB, Olney AH, Tamayo M, Frías JL. MacDonald MR, et al. Among authors: frias jl. Am J Med Genet. 1993 Jul 1;46(6):706-11. doi: 10.1002/ajmg.1320460622. Am J Med Genet. 1993. PMID: 8362914

6

[Etiologic distribution of children with congenital defects].

Martínez Frías ML, Rodríguez Pinilla E, Bermejo Sánchez E, Urioste Azcorra M, Villa Milla A, Lorda Sánchez I, Frías JL. Martínez Frías ML, et al. Among authors: frias jl. An Esp Pediatr. 1996 Dec;45(6):635-8. An Esp Pediatr. 1996. PMID: 9133231 Spanish.

7

Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder.

Martínez-Frías ML, Martín M, Pardo M, Fernandez de las Heras F, Frías JL. Martínez-Frías ML, et al. Among authors: frias jl. Am J Med Genet. 1995 Jan 16;55(2):213-6. doi: 10.1002/ajmg.1320550212. Am J Med Genet. 1995. PMID: 7717420

8

Kabuki make-up (Niikawa-Kuroki) syndrome in five Spanish children.

Galán-Gómez E, Cardesa-García JJ, Campo-Sampedro FM, Salamanca-Maesso C, Martínez-Frías ML, Frías JL. Galán-Gómez E, et al. Among authors: frias jl. Am J Med Genet. 1995 Nov 20;59(3):276-82. doi: 10.1002/ajmg.1320590303. Am J Med Genet. 1995. PMID: 8599349 Review.

9

Errors of morphogenesis and developmental field theory.

Martínez-Frías ML, Frías JL, Opitz JM. Martínez-Frías ML, et al. Among authors: frias jl. Am J Med Genet. 1998 Apr 1;76(4):291-6. Am J Med Genet. 1998. PMID: 9545092 Review.

10

Facial morphometry of Ecuadorian patients with growth hormone receptor deficiency/Laron syndrome.

Schaefer GB, Rosenbloom AL, Guevara-Aguirre J, Campbell EA, Ullrich F, Patil K, Frias JL. Schaefer GB, et al. Among authors: frias jl. J Med Genet. 1994 Aug;31(8):635-9. doi: 10.1136/jmg.31.8.635. J Med Genet. 1994. PMID: 7815422 Free PMC article.

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