Gabarrón J - Search Results

1

Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families.

Milà M, Kruyer H, Glover G, Sánchez A, Carbonell P, Castellví-Bell S, Volpini V, Rossell J, Gabarrón J, López I, et al. Milà M, et al. Among authors: gabarron j. Hum Genet. 1994 Oct;94(4):395-400. doi: 10.1007/BF00201600. Hum Genet. 1994. PMID: 7927336

2

Fragile X screening program in a Spanish region.

Gabarrón J, Lopez I, Glover G, Carbonell P. Gabarrón J, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):333-8. doi: 10.1002/ajmg.1320430151. Am J Med Genet. 1992. PMID: 1605207

3

FRAXE mutation analysis in three Spanish families.

Carbonell P, López I, Gabarrón J, Bernabé MJ, Lucas JM, Guitart M, Gabau E, Glover G. Carbonell P, et al. Among authors: gabarron j. Am J Med Genet. 1996 Aug 9;64(2):434-40. doi: 10.1002/(SICI)1096-8628(19960809)64:2<434::AID-AJMG40>3.0.CO;2-D. Am J Med Genet. 1996. PMID: 8844099

4

Partial monosomy 6q(q15q21) by de novo interstitial deletion.

Glover G, López I, Gabarrón J, Carmona JA. Glover G, et al. Among authors: gabarron j. Clin Genet. 1988 Apr;33(4):308-10. doi: 10.1111/j.1399-0004.1988.tb03453.x. Clin Genet. 1988. PMID: 3359687

5

De novo 10q(q21q22) interstitial deletion.

Glover G, Gabarrón J, López Ballester JA. Glover G, et al. Among authors: gabarron j. Hum Genet. 1987 Jun;76(2):205. doi: 10.1007/BF00284924. Hum Genet. 1987. PMID: 3610151

6

Chromosomal imbalance in the offspring of translocation carriers involving 7p. Further contribution with three cases to the partial trisomy 7p phenotype.

Gabarrón J, Glover G, Jiménez A, Salas P, Pérez-Bryan J, Parra MJ. Gabarrón J, et al. Clin Genet. 1988 Mar;33(3):211-9. doi: 10.1111/j.1399-0004.1988.tb03439.x. Clin Genet. 1988. PMID: 3359679

7

Premature centromere division dominantly inherited in a subfertile family.

Gabarrón J, Jimenez A, Glover G. Gabarrón J, et al. Cytogenet Cell Genet. 1986;43(1-2):69-71. doi: 10.1159/000132299. Cytogenet Cell Genet. 1986. PMID: 3780318

8

Pseudoisodicentric bisatellited extra marker chromosome (tetrasomy 22pter----q11, trisomy Yqh), derived from a maternal Y/22 translocation. Association between this tetrasomy and "cat eye" phenotypical features.

Gabarrón J, Glover G, Jimenez A, Lamata E. Gabarrón J, et al. Clin Genet. 1985 Dec;28(6):509-15. doi: 10.1111/j.1399-0004.1985.tb00418.x. Clin Genet. 1985. PMID: 3865751

9

Prenatal diagnosis in Spain.

Gabarrón J, Ramos C. Gabarrón J, et al. Eur J Hum Genet. 1997;5 Suppl 1:64-9. Eur J Hum Genet. 1997. PMID: 9101183

10

[Partial 7p trisomy. Report of new phenotype features].

Román Ortiz E, López-Sánchez-Solís de Querol M, Peris-Mencheta Ríos-Melida MD, Pajarón de Ahumada M, Gracian Gómez M, Guia Torrent JM, Fernández Parra R, Martínez-Artero Martínez I, Gabarrón J, Salvat Germán F. Román Ortiz E, et al. Among authors: gabarron j. An Esp Pediatr. 1992 Jan;36(1):62-4. An Esp Pediatr. 1992. PMID: 1543296 Spanish. No abstract available.

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