Search Results - Galutira, D

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  1. 1
    Identical twins discordant for multiple sclerosis have a shift in their T‐cell receptor repertoires

    Identical twins discordant for multiple sclerosis have a shift in their T‐cell receptor repertoires by HAEGERT, D. G., GALUTIRA, D., MURRAY, T. J., O'CONNOR, P., GADAG, V.

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  2. 2
    Identical twins discordant for multiple sclerosis have a shift in their T-cell recetor repertoires

    Identical twins discordant for multiple sclerosis have a shift in their T-cell recetor repertoires by Haegert, D G, Galutira, D, Murray, T J, O'Connor, P, Gadag, V

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  3. 3
    HaeIII RFLP for salivary proline-rich protein gene probe (pPRPII2.2RP)

    HaeIII RFLP for salivary proline-rich protein gene probe (pPRPII2.2RP) by GALUTIRA, D, ALLDERDICE, P. W, DAVIDSON, W. S

    Published in Nucleic acids research
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  4. 4
    HaelII RFLP for salivary proline-rich protein gene probe (pPRPII2.2RP)

    HaelII RFLP for salivary proline-rich protein gene probe (pPRPII2.2RP) by Galutira, D., Allderdice, P.W., Davidson, W.S.

    Published in Nucleic acids research
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  5. 5
    The genetic architecture of Stargardt macular dystrophy (STGD1): a longitudinal 40-year study in a genetic isolate

    The genetic architecture of Stargardt macular dystrophy (STGD1): a longitudinal 40-year study in a genetic isolate by Green, Jane S, O'Rielly, Darren D, Pater, Justin A, Houston, Jim, Rajabi, Hoda, Galutira, Dante, Benteau, Tammy, Sheaves, Amy, Abdelfatah, Nelly, Bautista, Donna, Whelan, Jim, Young, Terry-Lynn

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  6. 6
    A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene

    A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene by Abdelfatah, Nelly, Mostafa, Ahmed A., French, Curtis R., Doucette, Lance P., Penney, Cindy, Lucas, Matthew B., Griffin, Anne, Booth, Valerie, Rowley, Christopher, Besaw, Jessica E., Tranebjærg, Lisbeth, Rendtorff, Nanna Dahl, Hodgkinson, Kathy A., Little, Leichelle A., Agrawal, Sumit, Parnes, Lorne, Batten, Tony, Moore, Susan, Hu, Pingzhao, Pater, Justin A., Houston, Jim, Galutira, Dante, Benteau, Tammy, MacDonald, Courtney, French, Danielle, O’Rielly, Darren D., Stanton, Susan G., Young, Terry-Lynn

    Published in Human genetics
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  7. 7
    Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

    Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 by Doucette, Lance, Merner, Nancy D, Cooke, Sandra, Ives, Elizabeth, Galutira, Dante, Walsh, Vanessa, Walsh, Tom, MacLaren, Linda, Cater, Tracey, Fernandez, Bridget, Green, Jane S, Wilcox, Edward R, Shotland, Larry, Li, X C, Lee, Ming, King, Mary-Claire, Young, Terry-Lynn

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  8. 8
    A Cross-Cultural Validation of a Quality of Life Measure Using the Simple Measure of the Impact of Lupus Erythematosus in Youngsters (SMILEY©) among Filipino Pediatric Lupus Patients

    A Cross-Cultural Validation of a Quality of Life Measure Using the Simple Measure of the Impact of Lupus Erythematosus in Youngsters (SMILEY©) among Filipino Pediatric Lupus Patien... by Punzalan, Jemely M., Canonigo, Beatrice B., Cabansag, Maria Rosario F., Flores, Dennis S., Galutira, Paul Joseph T., Bernal, Christine B., Chan, Remedios D.

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  9. 9
    Erratum: Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

    Erratum: Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 by Doucette, Lance, Merner, Nancy D, Cooke, Sandra, Ives, Elizabeth, Galutira, Dante, Walsh, Vanessa, Walsh, Tom, MacLaren, Linda, Cater, Tracey, Fernandez, Bridget, Green, Jane S, Wilcox, Edward R, Shotland, Larry, Li, X C, Lee, Ming, King, Mary-Claire, Young, Terry-Lynn

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  10. 10
    Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

    Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 by Doucette, Lance, Merner, Nancy D, Cooke, Sandra, Ives, Elizabeth, Galutira, Dante, Walsh, Vanessa, Walsh, Tom, Maclaren, Linda, Cater, Tracey, Fernandez, Bridget, Green, Jane S, Wilcox, Edward R, Shotland, Larry, Li, X C, Lee, Ming, King, Mary-claire, Young, Terry-lynn

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