Search Results - Bautista-Llácer, R

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  1. 1
    Birth of a healthy boy after PGD for X-linked heterotaxy syndrome

    Birth of a healthy boy after PGD for X-linked heterotaxy syndrome by Bautista-Llácer, R., Pardo-Belenguer, M., García-Mengual, E., Sánchez-Matamoros, C., Raga, E., Calafell, J. M., Cívico, M. S., Fábregues, F., Vendrell, X.

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  2. 2
    P-22 Revisiting aneuploidy in spermatozoa as a PGS indication: How many sperm chromosomes should be analyzed?

    P-22 Revisiting aneuploidy in spermatozoa as a PGS indication: How many sperm chromosomes should be analyzed? by Vendrell, X, García-Mengual, E, Sánchez-Matamoros, C, Sánchez, E, Pardo, M, Bautista-Llácer, R, Raga, E, Alberola, T.M

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  3. 3
    P-40 Combined molecular and chromosomal analysis in embryos: Our experience

    P-40 Combined molecular and chromosomal analysis in embryos: Our experience by Alberola, T.M, Bautista-Llácer, R, Pardo, M, Sánchez-Matamoros, C, García-Mengual, E, Vendrell, X

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  4. 4
    DrosDel deletion collection: a Drosophila genomewide chromosomal deficiency resource

    DrosDel deletion collection: a Drosophila genomewide chromosomal deficiency resource by Ryder, E, Ashburner, M, Bautista-Llacer, R, Drummond, J, Webster, J, Johnson, G, Morley, T, Chan, Y.S, Blows, F, Coulson, D

    Published in Genetics (Austin)
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  5. 5
    DrosDel collection: a set of P-element insertions for generating custom chromosomal aberrations in Drosophila melanogaster

    DrosDel collection: a set of P-element insertions for generating custom chromosomal aberrations in Drosophila melanogaster by Ryder, E, Blows, F, Ashburner, M, Bautista-Llacer, R, Coulson, D, Drummond, J, Webster, J, Gubb, D, Gunton, N, Johnson, G

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  6. 6
    Is whole genome amplification really offering advantages to traditional nested fluorescent PCR amplification in single cells as promised?

    Is whole genome amplification really offering advantages to traditional nested fluorescent PCR amplification in single cells as promised? by Alberola, TM, Bautista-Llácer, R, Vendrell, X, Pérez-Alonso, M

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  7. 7
    PGD for Wiskott–Aldrich syndrome in a family where only carrier women were available and where crossover was detected in the preclinical study

    PGD for Wiskott–Aldrich syndrome in a family where only carrier women were available and where crossover was detected in the preclinical study by Alberola, TM, Bautista-Llácer, R, Pardo, M, Boada, M, Parriego, M, Veiga, A, Vendrell, X, Pérez-Alonso, M

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