The down-up bone bridge approach for cochlear and middle ear implants: Our experience in 34 patients von Achena, F., Montaldo, C., Nucaro, A.L.

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Chromosome 8p23.2-pter: a critical region for mental retardation, autism and epilepsy? von Nucaro, A, Pisano, T, Chillotti, I, Montaldo, C, Pruna, D

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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

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Frequency of the thiopurine S-methyltransferase alleles in the ancient genetic population isolate of Sardinia von Rossino, R., Vincis, C., Alves, S., Prata, M. J., Macis, M. D., Nucaro, A. L., Schirru, E., Congia, M.

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New case of contiguous gene syndrome at chromosome 8p11.2p12 von Cau, M., Congiu, R., Origa, R., Galanello, R., Melis, M.A., Nucaro, A.L.

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Microbial Changes in Subgingival Plaque and Polymicrobial Intracellular Flora in Buccal Cells after Fixed Orthodontic Appliance Therapy: A Preliminary Study von Montaldo, Caterina, Erriu, Matteo, Giovanna Pili, Francesca Maria, Peluffo, Carla, Nucaro, Annalisa, Orrù, Germano, Denotti, Gloria

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Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism von COSSU, P, PIRASTU, M, NUCARO, A, FIGUS, A, BALESTRIERI, A, BORRONE, C, GIACCHINO, R, DEVOTO, M, MONNI, G, CAO, A

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DNA‐BASED DIAGNOSIS OF WILSON DISEASE von Holmes, Ronald, Cossu, P, Pirastu, M, Nucaro, A

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Pseudomosaic centric fission of chromosome 4 in amniotic cells von Nucaro, A., Falchi, A. M., Monni, G., Cao, A.

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

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Iron overload and desferrioxamine chelation therapy in beta-thalassemia intermedia von Cossu, P, Toccafondi, C, Vardeu, F, Sanna, G, Frau, F, Lobrano, R, Cornacchia, G, Nucaro, A, Bertolino, F, Loi, A, De Virgiliis, S, Cao, A

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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

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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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Acute lymphoblastic leukemia in a child with constitutional ring chromosome 21 von Falchi, Angela M., Orofino, Maria G., Nucaro, Anna L., De Virgiliis, Stefano, Cao, Antonio

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PHARMACOGENETICS: Frequency of the thiopurine S-methyltransferase alleles in the ancient genetic population isolate of Sardinia von Rossino, R, Vincis, C, Alves, S, Prata, MJ, Macis, MD, Nucaro, AL, Schirru, E, Congia, M

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X-linked mental retardation and characteristic physical features in two brothers with duplication Xp22-Xpter von Cianchetti, Carlo, Muntoni, Francesco, Falchi, Angela-Maria, Nucaro, Annalisa, Sannio-Fancello, Giuseppina, Cao, Antonio, Marrosu, Maria-Giovanna

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Chromosome 8p23.2-pter: a critical region for mental retardation, autism and epilepsy? von Nucaro, A, Pisano, T, Chillotti, I, Montaldo, C, Pruna, D

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DNA-BASED DIAGNOSIS OF WILSON DISEASE von Holmes, Ronald, P, Cossu, M, Pirastu, A, Nucaro

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New case of contiguous gene syndrome at chromosome 8p11.2p12 von Cau, M, Congiu, R, Origa, R, Galanello, R, Melis, M A, Nucaro, A L

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X-LINKED MENTAL-RETARDATION AND CHARACTERISTIC PHYSICAL FEATURES IN 2 BROTHERS WITH DUPLICATION XP22-XPTER von CIANCHETTI, C, MUNTONI, F, FALCHI, AM, NUCARO, A, SANNIOFANCELLO, G, CAO, A, MARROSU, MG

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