Benavides A - Search Results

1

PCR-based study of the presence of Y-chromosome sequences in patients with Ullrich-Turner syndrome.

Coto E, Toral JF, Menéndez MJ, Hernando I, Plasencia A, Benavides A, López-Larrea C. Coto E, et al. Among authors: benavides a. Am J Med Genet. 1995 Jul 3;57(3):393-6. doi: 10.1002/ajmg.1320570305. Am J Med Genet. 1995. PMID: 7677140

2

[Cystic fibrosis in Asturias: an elevated frequency of the delta F508 mutation].

Coto E, Bousoño C, Menéndez MJ, Cue R, Toral JF, Benavides A, Hernando I, Plasencia A, López-Larrea C. Coto E, et al. Among authors: benavides a. Med Clin (Barc). 1994 Nov 26;103(18):681-3. Med Clin (Barc). 1994. PMID: 7808073 Spanish.

3

[Diagnosis of dominant renal polycystosis in adults by analysis of DNA polymorphism].

Coto E, Aguado S, Alvarez J, Sanz de Castro S, Arias M, Fernández Toral J, Benavides A, Hernando I, Plasencia A, Herrera J, et al. Coto E, et al. Among authors: benavides a. Med Clin (Barc). 1992 Mar 21;98(11):409-12. Med Clin (Barc). 1992. PMID: 1349048 Spanish.

4

A labor and cost effective next generation sequencing of PKHD1 in autosomal recessive polycystic kidney disease patients.

Tavira B, Gómez J, Málaga S, Santos F, Fernández-Aracama J, Alonso B, Iglesias S, Benavides A, Hernando I, Plasencia A, Alvarez V, Coto E. Tavira B, et al. Among authors: benavides a. Gene. 2015 Apr 25;561(1):165-9. doi: 10.1016/j.gene.2015.02.040. Epub 2015 Feb 17. Gene. 2015. PMID: 25701400

5

[Basan's syndrome: dominant autosomal hypohidrotic ectodermal dysplasia].

Hernando I, Benavides A, Plasencia A, Visus EP, Bousoño C, Fernández Toral J. Hernando I, et al. Among authors: benavides a. An Esp Pediatr. 1988 Apr;28(4):359-60. An Esp Pediatr. 1988. PMID: 3400948 Spanish. No abstract available.

6

[Amniotic band syndrome and a 47, XYY karyotype].

Hernando I, Plasencia A, Peña E, Fernández Pérez M, Benavides A, Rodríguez de la Rúa MV, Fernández Toral J. Hernando I, et al. Among authors: benavides a. An Esp Pediatr. 1987 Jul;27(1):75-6. An Esp Pediatr. 1987. PMID: 3662260 Spanish. No abstract available.

7

[National program of prenatal diagnosis].

Benavides A, Llavero J, Hernando I. Benavides A, et al. An Esp Pediatr. 1988 Sep;29 Suppl 33:192-4. An Esp Pediatr. 1988. PMID: 3250290 Spanish. No abstract available.

8

[Mental retardation and X chromosome fragility].

Rodríguez de la Rúa V, Alvárez García F, Hernando I, Benavides A, Coto GD, de Juan J, Fernández Toral J. Rodríguez de la Rúa V, et al. Among authors: benavides a. An Esp Pediatr. 1986 Nov;25(5):329-34. An Esp Pediatr. 1986. PMID: 3813225 Spanish.

9

An outbreak of Legionnaires' disease in an inner city district: importance of the first 24 hours in the investigation.

Jansà JM, Caylà JA, Ferrer D, Gracia J, Pelaz C, Salvador M, Benavides A, Pellicer T, Rodriguez P, Garcés JM, Segura A, Guix J, Plasencia A; Barcelona Legionellosis Study Group. Jansà JM, et al. Among authors: benavides a. Int J Tuberc Lung Dis. 2002 Sep;6(9):831-8. Int J Tuberc Lung Dis. 2002. PMID: 12234140

10

[Karyotype in GPG bands: description of a elementaly technique for routine (author's transl)].

Fernández Toral J, Barreiro J, Benavides A, Bousoño C, Crespo M. Fernández Toral J, et al. Among authors: benavides a. An Esp Pediatr. 1980 Aug;13(8):700-3. An Esp Pediatr. 1980. PMID: 7436150 Spanish.

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