Treffer 1 - 12 von 12 für Suche 'Nucaro, Anna Lisa', Suchdauer: 1,25s Treffer weiter einschränken
  1. 1
    Cryptic chromosome rearrangements in five patients, with normal and/or abnormal karyotypes, associated with mental retardation, autism and/or epilepsy, detected by BAC genome array-CGH

    Cryptic chromosome rearrangements in five patients, with normal and/or abnormal karyotypes, associated with mental retardation, autism and/or epilepsy, detected by BAC genome array... von Cabras, V, Milia, A, Montaldo, C, Nucaro, A

    Veröffentlicht in Prague medical report

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  2. 2
    Ring 20 syndrome mosaicism and epilepsy: a case with duplication of two BAC clones in 20q11.21-q11.22 defined by genome array-CGH

    Ring 20 syndrome mosaicism and epilepsy: a case with duplication of two BAC clones in 20q11.21-q11.22 defined by genome array-CGH von Cabras, Valentina, Erriu, Matteo, Loi, Mario, Milia, Angela, Montaldo, Caterina, Nucaro, Anna Lisa

    Veröffentlicht in Journal of clinical pathology

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  3. 3
    Ring chromosome 14 mosaicism: An unusual case associated with developmental delay and epilepsy, characterized by genome array-CGH

    Ring chromosome 14 mosaicism: An unusual case associated with developmental delay and epilepsy, characterized by genome array-CGH von Nucaro, Anna Lisa, Falchi, Melania, Pisano, Tiziana, Rossino, Rossano, Boscarelli, Francesca, Stoico, Giusi, Milia, Angela, Montaldo, Caterina, Cianchetti, Carlo, Pruna, Dario


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  4. 4
    Prenatal diagnosis of a mosaic supernumerary marker iso (8p) (tetrasomy 8p): discordance between chorionic villi culture and amniotic fluid karyotypes

    Prenatal diagnosis of a mosaic supernumerary marker iso (8p) (tetrasomy 8p): discordance between chorionic villi culture and amniotic fluid karyotypes von Nucaro, Anna Lisa, Rossino, Rossano, Pruna, Dario, Rassu, Stefania, Cianchetti, Carlo, Cao, Antonio, Moi, Paolo

    Veröffentlicht in Prenatal diagnosis

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  5. 5
    Familial translocation t(3;10) (p26.3;p12.31) leading to trisomy 10p12.31 → pter and monosomy 3p26.3 → pter in seven members

    Familial translocation t(3;10) (p26.3;p12.31) leading to trisomy 10p12.31 → pter and monosomy 3p26.3 → pter in seven members von Nucaro, Anna Lisa, Meloni, Marta, Pisano, Tiziana, Melis, Paola, Rossi, Elena, Rossino, Rossano, Corona, Simona, Loi, Mario, Achena, Francesco, Zuffardi, Orsetta, Cianchetti, Carlo


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  6. 6
    Familial translocation t(3; 10) (p26.3; p12.31) leading to trisomy 10p12.31 Delta RT pter and monosomy 3p26.3 Delta RT pter in seven members

    Familial translocation t(3; 10) (p26.3; p12.31) leading to trisomy 10p12.31 Delta RT pter and monosomy 3p26.3 Delta RT pter in seven members von Nucaro, Anna Lisa, Meloni, Marta, Pisano, Tiziana, Melis, Paola, Rossi, Elena, Rossino, Rossano, Corona, Simona, Loi, Mario, Achena, Francesco, Zuffardi, Orsetta, Cianchetti, Carlo


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  7. 7
    Prenatal diagnosis of a double trisomy 48, XXY, +13: Klinefelter and Patau syndromes

    Prenatal diagnosis of a double trisomy 48, XXY, +13: Klinefelter and Patau syndromes von Rossino, Rossano, Nucaro, Anna Lisa


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  8. 8
    Turner syndrome mosaicism: an unusual case with a de novo large dicentric marker chromosome: mos 45,X/46,X, ter rea(X;X)(p22.3;p22.3)

    Turner syndrome mosaicism: an unusual case with a de novo large dicentric marker chromosome: mos 45,X/46,X, ter rea(X;X)(p22.3;p22.3) von Nucaro, Anna Lisa, Melis, Paola, Casini, Maria Rosaria, Rossino, Rossano, Cau, Milena, Melis, Maria Antonietta, Loche, Sandro

    Veröffentlicht in Journal of applied genetics

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  9. 9
    Trisomy 8 mosaicism in a patient born to a mother with 47,XXX

    Trisomy 8 mosaicism in a patient born to a mother with 47,XXX von Nucaro, Anna Lisa, Cao, Antonio, Faedda, Antonella, Crisponi, Giangiorgio


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  10. 10
    Prenatal diagnosis of a double trisomy 48, XXY, +13: Klinefelter and Patau syndromes

    Prenatal diagnosis of a double trisomy 48, XXY, +13: Klinefelter and Patau syndromes von Rossino, Rossano, Nucaro, Anna Lisa


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  11. 11
    Ring 20 syndrome mosaicism and epilepsy: a case with duplication of two BAC clones in 20q11.21-q11.22 defined by genome array-CGH

    Ring 20 syndrome mosaicism and epilepsy: a case with duplication of two BAC clones in 20q11.21-q11.22 defined by genome array-CGH von Cabras, Valentina, Erriu, Matteo, Loi, Mario, Milia, Angela, Montaldo, Caterina, Nucaro, Anna Lisa

    Veröffentlicht in Journal of clinical pathology

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  12. 12
    Trisomy 8 mosaicism in a patient born to a mother with 47,XXX

    Trisomy 8 mosaicism in a patient born to a mother with 47,XXX von Nucaro, Anna Lisa, Cao, Antonio, Faedda, Antonella, Crisponi, Giangiorgio


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