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[Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations].
Nájera C, Sánchez F, Mateu E, Prieto F, Beneyto M. Nájera C, et al. Med Clin (Barc). 2001 Mar 17;116(10):365-72. doi: 10.1016/s0025-7753(01)71832-5. Med Clin (Barc). 2001. PMID: 11333669 Spanish.
Genetics of retinoblastoma: a study.
Mateu E, Sánchez F, Nájera C, Beneyto M, Castell V, Hernández M, Serra I, Prieto F. Mateu E, et al. Cancer Genet Cytogenet. 1997 May;95(1):40-50. doi: 10.1016/s0165-4608(96)00387-1. Cancer Genet Cytogenet. 1997. PMID: 9140452
Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCR.
Valero R, Marfany G, Gil-Benso R, Ibáñez MA, López-Pajares I, Prieto F, Rullan G, Sarret E, Gonzàlez-Duarte R. Valero R, et al. J Med Genet. 1999 Sep;36(9):694-9. J Med Genet. 1999. PMID: 10507727 Free PMC article.
Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.
Martínez F, Martínez-Garay I, Millán JM, Pérez-Aytes A, Moltó MD, Orellana C, Prieto F. Martínez F, et al. Am J Med Genet. 2001 Aug 1;102(2):200-4. doi: 10.1002/ajmg.1416. Am J Med Genet. 2001. PMID: 11477616
Genetic localisation of mental retardation with spastic diplegia to the pericentromeric region of the X chromosome: X inactivation in female carriers.
Martínez F, Tomás M, Millán JM, Fernández A, Palau F, Prieto F. Martínez F, et al. J Med Genet. 1998 Apr;35(4):284-7. doi: 10.1136/jmg.35.4.284. J Med Genet. 1998. PMID: 9598720 Free PMC article.
Localization of MRX82: a new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family.
Martínez F, Martínez-Garay I, Oltra S, Moltó MD, Orellana C, Monfort S, Prieto F, Tejada I. Martínez F, et al. Am J Med Genet A. 2004 Dec 1;131(2):174-8. doi: 10.1002/ajmg.a.30352. Am J Med Genet A. 2004. PMID: 15526294
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