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Pardo-Manuel de Villena, F; de la Casa-Esperon, E; Briscoe, T L et al. (2000) A genetic test to determine the origin of maternal transmission ratio distortion. Meiotic drive at the mouse Om locus. Genetics 154:333-42
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de la Casa-Esperon, E; Pardo-Manuel de Villena, F; Verner, A E et al. (2000) Sex-of-offspring-specific transmission ratio distortion on mouse chromosome X. Genetics 154:343-50
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Pardo-Manuel De Villena, F; de La Casa-Esperon, E; Williams, J W et al. (2000) Heritability of the maternal meiotic drive system linked to Om and high-resolution mapping of the Responder locus in mouse. Genetics 155:283-9
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Pardo-Manuel de Villena, F; de la Casa-Esperon, E; Verner, A et al. (1999) The maternal DDK syndrome phenotype is determined by modifier genes that are not linked to Om. Mamm Genome 10:492-7
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Naumova, A K; Olien, L; Bird, L M et al. (1998) Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human. Eur J Hum Genet 6:552-62
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Naumova, A K; Leppert, M; Barker, D F et al. (1998) Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome. Am J Hum Genet 62:1493-9
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Latham, K E; Sapienza, C (1998) Localization of genes encoding egg modifiers of paternal genome function to mouse chromosomes one and two. Development 125:929-35
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Pardo-Manuel de Villena, F; Naumova, A K; Verner, A E et al. (1997) Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal ""DDK syndrome"" genes are linked. Mamm Genome 8:642-6
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Pardo-Manual de Villena, F; Slamka, C; Fonseca, M et al. (1996) Transmission-ratio distortion through F1 females at chromosome 11 loci linked to Om in the mouse DDK syndrome. Genetics 142:1299-304
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Pardo-Manuel de Villena, F; Sapienza, C (1996) Genetic mapping of DXYMov15-associated sequences in the pseudoautosomal region of the C57BL/6J strain. Mamm Genome 7:237-9
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Showing the most recent 10 out of 11 publications
