Benitez J - Search Results

1

Homozygous myotonic dystrophy: clinical and molecular studies of three unrelated cases.

Martorell L, Illa I, Rosell J, Benitez J, Sedano MJ, Baiget M. Martorell L, et al. Among authors: benitez j. J Med Genet. 1996 Sep;33(9):783-5. doi: 10.1136/jmg.33.9.783. J Med Genet. 1996. PMID: 8880582 Free PMC article.

2

Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families.

Bayés M, Valverde D, Balcells S, Grinberg D, Vilageliu L, Benítez J, Ayuso C, Beneyto M, Baiget M, Gonzàlez-Duarte R. Bayés M, et al. Among authors: benitez j. Hum Genet. 1995 Jul;96(1):89-94. doi: 10.1007/BF00214192. Hum Genet. 1995. PMID: 7607661

3

Prevalence of BRCA1 and BRCA2 Jewish mutations in Spanish breast cancer patients.

Díez O, Osorio A, Robledo M, Barroso A, Domènech M, Cortés J, Albertos J, Sanz J, Brunet J, SanRomán JM, Alonso MC, Baiget M, Benítez J. Díez O, et al. Among authors: benitez j. Br J Cancer. 1999 Mar;79(7-8):1302-3. doi: 10.1038/sj.bjc.6690208. Br J Cancer. 1999. PMID: 10098775 Free PMC article.

4

Molecular analysis of the six most recurrent mutations in the BRCA1 gene in 87 Spanish breast/ovarian cancer families.

Osorio A, Robledo M, Albertos J, Díez O, Alonso C, Baiget M, Benítez J. Osorio A, et al. Among authors: benitez j. Cancer Lett. 1998 Jan 30;123(2):153-8. doi: 10.1016/s0304-3835(97)00416-3. Cancer Lett. 1998. PMID: 9489482

5

[Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics].

Benítez J, Fernández E, Ramos C, Nunes V, del Río E, Baiget M. Benítez J, et al. Rev Clin Esp. 1989 Apr;184(7):364-6. Rev Clin Esp. 1989. PMID: 2570446 Spanish.

6

Homozygous tandem duplication within the gene encoding the beta-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa.

Bayés M, Giordano M, Balcells S, Grinberg D, Vilageliu L, Martínez I, Ayuso C, Benítez J, Ramos-Arroyo MA, Chivelet P, et al. Bayés M, et al. Among authors: benitez j. Hum Mutat. 1995;5(3):228-34. doi: 10.1002/humu.1380050307. Hum Mutat. 1995. PMID: 7599633

7

Novel rhodopsin mutation in an autosomal dominant retinitis pigmentosa family: phenotypic variation in both heterozygote and homozygote Val137Met mutant patients.

Ayuso C, Trujillo MJ, Robledo M, Ramos C, Benitez J, Martín-Osés F, del Rio T, García-Sandoval B. Ayuso C, et al. Among authors: benitez j. Hum Genet. 1996 Jul;98(1):51-4. doi: 10.1007/s004390050158. Hum Genet. 1996. PMID: 8682506

8

Ring chromosome 6: clinical and cytogenetic behaviour.

Paz-y-Miño C, Benítez J, Ayuso C, Sánchez-Cascos A. Paz-y-Miño C, et al. Among authors: benitez j. Am J Med Genet. 1990 Apr;35(4):481-3. doi: 10.1002/ajmg.1320350407. Am J Med Genet. 1990. PMID: 2333874

9

[Prenatal diagnosis of hemophilia A by DNA analysis. First experience in Spain].

Baiget M, Nunes V, del Río E, Ramos C, Ayuso C, Benítez J, Díaz Recasens J. Baiget M, et al. Among authors: benitez j. Med Clin (Barc). 1987 May 16;88(19):770-2. Med Clin (Barc). 1987. PMID: 3613722 Spanish. No abstract available.

10

High prevalence of the C634Y mutation in the RET proto-oncogene in MEN 2A families in Spain.

Sánchez B, Robledo M, Biarnes J, Sáez ME, Volpini V, Benítez J, Navarro E, Ruiz A, Antiñolo G, Borrego S. Sánchez B, et al. Among authors: benitez j. J Med Genet. 1999 Jan;36(1):68-70. J Med Genet. 1999. PMID: 9950371 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,668 results

Search Page

Filters