Search Results - Hassed, SJ

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  1. 1
    A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome

    A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome by Hassed, SJ, Hopcus-Niccum, D, Zhang, L, Li, S, Mulvihill, JJ

    Published in Clinical genetics
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  2. 2
    Chromosome 2q terminal deletion: Report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals

    Chromosome 2q terminal deletion: Report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals by Casas, Kari A., Mononen, Tarja K., Mikail, Claudia N., Hassed, Susan J., Li, Shibo, Mulvihill, John J., Lin, Henry J., Falk, Rena E.

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  3. 3
    The effects of peer ridicule on depression and self-image among adolescent females with Turner syndrome

    The effects of peer ridicule on depression and self-image among adolescent females with Turner syndrome by RICKERT, V. I, HASSED, S. J, HENDON, A. E, CUNNIFF, C

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  4. 4
    High-resolution cytogenetic characterization of telomeric associations in ring chromosome 19

    High-resolution cytogenetic characterization of telomeric associations in ring chromosome 19 by SAWYER, J. R, ROWE, R. A, HASSED, S. J, CUNNIFF, C

    Published in Human genetics
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  5. 5
    Blepharophimosis: A causally heterogeneous malformation frequently associated with developmental disabilities

    Blepharophimosis: A causally heterogeneous malformation frequently associated with developmental disabilities by Cunniff, Christopher, Curtis, Mary, Hassed, Susan J., Hoyme, H. Eugene

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  6. 6
    Telomeric fusion and chromosome instability in multiple tissues of a patient with mosaic Ullrich-Turner syndrome

    Telomeric fusion and chromosome instability in multiple tissues of a patient with mosaic Ullrich-Turner syndrome by Sawyer, Jeffrey R., Swanson, Charles M., Lukacs, Janet L., Hassed, Susan J., Curtis, Mary A., North, Paula E., Kozlowski, Karen J., Pihoker, Catherine

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