Ayuso C - Search Results

1

Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded child.

Lorda-Sanchez I, Lopez-Pajares I, Roche MC, Sanz R, Rodriguez de Alba M, Gonzalez-Gonzalez MC, Ibañez A, Ramos C, Ayuso C. Lorda-Sanchez I, et al. Among authors: ayuso c. Am J Med Genet. 2000 Dec 11;95(4):336-8. Am J Med Genet. 2000. PMID: 11186887

2

[DNA markers linked to Huntington's disease (D4S10 and D4S95) in Spanish families: preliminary results].

Benítez J, Ramos C, Fernández E, Ayuso C, Yébenes J. Benítez J, et al. Among authors: ayuso c. Rev Clin Esp. 1992 Apr;190(6):299-301. Rev Clin Esp. 1992. PMID: 1350862 Spanish.

3

Study of the parental origin of sexual aneuploidy in ten families using RFLPs.

Villamar M, Fernandez E, Ayuso C, Ramos C, Benitez J. Villamar M, et al. Among authors: ayuso c. Ann Genet. 1990;33(1):29-31. Ann Genet. 1990. PMID: 1973343

4

Parental origin of chromosomal nondisjunction in a 49,XXXXY male using recombinant-DNA techniques.

Villamar M, Benitez J, Fernández E, Ayuso C, Ramos C. Villamar M, et al. Among authors: ayuso c. Clin Genet. 1989 Sep;36(3):152-5. doi: 10.1111/j.1399-0004.1989.tb03181.x. Clin Genet. 1989. PMID: 2791329

5

[Role of the cytogeneticist in genetic counseling].

Sánchez Cascos A, Ayuso C, Ramos C. Sánchez Cascos A, et al. Among authors: ayuso c. An Esp Pediatr. 1988 Sep;29 Suppl 32:71-3. An Esp Pediatr. 1988. PMID: 3247972 Spanish. No abstract available.

6

Frequency of constitutional chromosome alterations in patients with hematologic neoplasias.

Benitez J, Valcarcel E, Ramos C, Ayuso C, Cascos AS. Benitez J, et al. Among authors: ayuso c. Cancer Genet Cytogenet. 1987 Feb;24(2):345-54. doi: 10.1016/0165-4608(87)90117-8. Cancer Genet Cytogenet. 1987. PMID: 3791180

7

Somatic stability in chorionic villi samples and other Huntington fetal tissues.

Benitez J, Robledo M, Ramos C, Ayuso C, Astarloa R, Garcia Yébenes J, Brambati B. Benitez J, et al. Among authors: ayuso c. Hum Genet. 1995 Aug;96(2):229-32. doi: 10.1007/BF00207386. Hum Genet. 1995. PMID: 7635477

8

Identification of a novel rhodopsin mutation (Met-44-Thr) in a simplex case of retinitis pigmentosa.

Reig C, Antich J, Gean E, Garcia-Sandoval B, Ramos C, Ayuso C, Carballo M. Reig C, et al. Among authors: ayuso c. Hum Genet. 1994 Sep;94(3):283-6. doi: 10.1007/BF00208284. Hum Genet. 1994. PMID: 8076945

9

Polymorphic variations in peripherin-RDS gene in the Spanish population.

Trujillo MJ, Ayuso C, Robledo M, Sandoval BG, Ramos C, Benitez J. Trujillo MJ, et al. Among authors: ayuso c. Ann Genet. 1995;38(4):225-7. Ann Genet. 1995. PMID: 8629810

10

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. Hum Genet. 1996 Jul;98(1):51-4. doi: 10.1007/s004390050158. Hum Genet. 1996. PMID: 8682506

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