Citation: Fpm. De Villena et C. Sapienza, Recombination is proportional to the number of chromosome arms in mammals, MAMM GENOME, 12(4), 2001, pp. 318-322
Citation: Fpm. De Villena et C. Sapienza, Transmission ratio distortion in offspring of heterozygous female carriersof Robertsonian translocations, HUM GENET, 108(1), 2001, pp. 31-36
Citation: Fpm. De Villena et C. Sapienza, Transmission of Robertsonian chromosomes through human female meiosis, CYTOG C GEN, 92(3-4), 2001, pp. 342-344
Authors:
de Villena, FPM
de la Casa-Esperon, E
Sapienza, C
Citation: Fpm. De Villena et al., Natural selection and the function of genome imprinting: beyond the silenced minority, TRENDS GEN, 16(12), 2000, pp. 573-579
Authors:
de Villena, FPM
de la Casa-Esperon, E
Williams, JW
Malette, JM
Rosa, M
Sapienza, C
Citation: Fpm. De Villena et al., Heritability of the maternal meiotic drive system linked to Om and high-resolution mapping of the Responder locus in mouse, GENETICS, 155(1), 2000, pp. 283-289
Authors:
de Villena, FPM
de la Casa-Esperon, E
Briscoe, TL
Sapienza, C
Citation: Fpm. De Villena et al., A genetic test to determine the origin of maternal transmission ratio distortion: Meiotic drive at the mouse Om locus, GENETICS, 154(1), 2000, pp. 333-342
Authors:
de la Casa-Esperon, E
de Villena, FPM
Verner, AE
Briscoe, TL
Malette, JM
Rosa, M
Jin, WH
Sapienza, C
Citation: E. De La Casa-esperon et al., Sex-of-offspring-specific transmission ratio distortion on mouse chromosome X, GENETICS, 154(1), 2000, pp. 343-350
Authors:
de Villena, FPM
de la Casa-Esperon, E
Briscoe, TL
Malette, JM
Sapienza, C
Citation: Fpm. De Villena et al., Male-offspring-specific, haplotype-dependent, nonrandom cosegregation of alleles at loci on two mouse chromosomes, GENETICS, 154(1), 2000, pp. 351-356
Authors:
de Villena, FPM
de la Casa-Esperon, E
Verner, A
Morgan, K
Sapienza, C
Citation: Fpm. De Villena et al., The maternal DDK syndrome phenotype is determined by modifier genes that are not linked to Om, MAMM GENOME, 10(5), 1999, pp. 492-497
Authors:
Naumova, AK
Olien, L
Bird, LM
Smith, M
Verner, AE
Leppert, M
Morgan, K
Sapienza, C
Citation: Ak. Naumova et al., Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human, EUR J HUM G, 6(6), 1998, pp. 552-562