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M G Miano

Showing results (1-10 of 17) with videos related to

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Clinical Genetics|June 28, 2007
A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palateF E Abidi, M G Miano, J C Murray, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian familyC Rozzo, M Fossarello, G Galleri, et al.
International Journal of Immunogenetics|April 14, 2006
A91V perforin variation in healthy subjects and FHLH patientsR Busiello, G Fimiani, M G Miano, et al.
Gene|April 1, 1997
Construction of a pilot human YAC library in a recombination-defective yeast strainG Palmieri, M G Miano, A Casamassimi, et al.
Human Reproduction (Oxford, England)|March 2, 2011
Nuclear factor-kappa-B-inhibitor alpha (NFKBIA) is a developmental marker of NF-κB/p65 activation during in vitro oocyte maturation and early embryogenesisM Paciolla, R Boni, F Fusco, et al.
The British Journal of Ophthalmology|November 3, 1998
Ocular signs associated with a rhodopsin mutation (Cys-167-->Arg) in a family with autosomal dominant retinitis pigmentosaF Simonelli, M Rinaldi, A Nesti, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1994
Sequence-tagged sites (STSs) from YAC insert-ends and X-specific flow-sorted chromosomesA Ciccodicola, C Cinti, T Esposito, et al.
Nature Genetics|August 10, 2000
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosaR Vervoort, A Lennon, A C Bird, et al.
European Journal of Endocrinology|October 7, 2000
The highly malignant phenotype of anaplastic thyroid carcinoma cell lines is recessiveM L Martelli, M G Miano, C Battaglia, et al.
Cancer Research|July 14, 1998
p53 genes mutated in the DNA binding site or at a specific COOH-terminal site exert divergent effects on thyroid cell growth and differentiationA Casamassimi, M G Miano, A Porcellini, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Clinical Genetics|June 28, 2007
A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palateF E Abidi, M G Miano, J C Murray, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian familyC Rozzo, M Fossarello, G Galleri, et al.
International Journal of Immunogenetics|April 14, 2006
A91V perforin variation in healthy subjects and FHLH patientsR Busiello, G Fimiani, M G Miano, et al.
Gene|April 1, 1997
Construction of a pilot human YAC library in a recombination-defective yeast strainG Palmieri, M G Miano, A Casamassimi, et al.
Human Reproduction (Oxford, England)|March 2, 2011
Nuclear factor-kappa-B-inhibitor alpha (NFKBIA) is a developmental marker of NF-κB/p65 activation during in vitro oocyte maturation and early embryogenesisM Paciolla, R Boni, F Fusco, et al.
The British Journal of Ophthalmology|November 3, 1998
Ocular signs associated with a rhodopsin mutation (Cys-167-->Arg) in a family with autosomal dominant retinitis pigmentosaF Simonelli, M Rinaldi, A Nesti, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1994
Sequence-tagged sites (STSs) from YAC insert-ends and X-specific flow-sorted chromosomesA Ciccodicola, C Cinti, T Esposito, et al.
Nature Genetics|August 10, 2000
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosaR Vervoort, A Lennon, A C Bird, et al.
European Journal of Endocrinology|October 7, 2000
The highly malignant phenotype of anaplastic thyroid carcinoma cell lines is recessiveM L Martelli, M G Miano, C Battaglia, et al.
Cancer Research|July 14, 1998
p53 genes mutated in the DNA binding site or at a specific COOH-terminal site exert divergent effects on thyroid cell growth and differentiationA Casamassimi, M G Miano, A Porcellini, et al.
Pageof 2