Search Results - "Spence, W C"

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    Molecular analysis of the rhd genotype in fetuses at risk for rhd hemolytic disease by Spence, W. Christine, Maddalena, Anne, Demers, Daniel B., Bick, David P.

    Published in Obstetrics and gynecology (New York. 1953) (01-02-1995)
    “…The objective of this study was to evaluate the accuracy of a DNA-based testing methodology in determining the RhD genotypes of fetuses at risk for RhD…”
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    The Human Bestiary by Spence, N. C. W.

    Published in The Modern language review (01-10-2001)
    “…This article studies the widespread application of animal names to human beings in the major languages of Western Europe. The phenomenon is common to all the…”
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    DNA-based prenatal determination of the RhEe genotype by Christine Spence, W., Potter, Phillip, Maddalena, Anne, Deniers, Daniel B., Bick, David P.

    Published in Obstetrics and gynecology (New York. 1953) (01-10-1995)
    “…Maternal antibodies to RhE may cause severe hemolytic disease. Based on recent RhD and RhCE sequence information, we have developed a DNA-based testing…”
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    Prenatal Determination of genotypes Kell and Cellano in at-risk pregnancies by SPENCE, W. C, MADDALENA, A, DEMERS, D. B, BICK, D. P

    Published in Journal of reproductive medicine (01-06-1997)
    “…To evaluate the accuracy of a DNA-based testing methodology in determining the KEL1 and KEL2 (Kell and Cellano) genotype of fetuses at risk for Kell or Cellano…”
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    Screening semen donors for hereditary diseases: The Fairfax cryobank experience by BICK, D, FUGGER, E. F, POOL, S. H, HAZELRIGG, W. B, YADVISH, K. N, SPENCE, W. C, MADDALENA, A, HOWARD-PEEBLES, P. N, SCHULMAN, J. D

    Published in Journal of reproductive medicine (01-05-1998)
    “…To study the carrier frequency of hereditary diseases in potential semen donors with no family history of a genetic disease. Carrier screening was performed on…”
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    Neonatal screening for cystic fibrosis: addition of molecular diagnostics to increase specificity by Spence, W C, Paulus-Thomas, J, Orenstein, D M, Naylor, E W

    Published in Biochemical medicine and metabolic biology (01-04-1993)
    “…Newborn screening for cystic fibrosis (CF) has been carried out on approximately 106,000 neonates in western Pennsylvania since 1987 using the immunoreactive…”
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    Psychosocial Characteristics of Institutionalized Adolescents: Resilient or at Risk? by Hutchinson, Roger L

    Published in Adolescence (1992)
    “…Attempted to provide psychosocial description of 187 institutionalized adolescents who completed Adolescent Health Inventory and Beck Depression Inventory…”
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    Identification of a 55-bp Deletion in the Glucocerebrosidase Gene in Gaucher Disease: Phenotypic Presentation and Implications for Mutation Detection Assays by Mao, Rong, O'Brien, John F., Rao, Subramanya, Schmitt, Eric, Roa, Benjamin, Feldman, Gerald L., Spence, W.Christine, Snow, Karen

    Published in Molecular genetics and metabolism (01-03-2001)
    “…A 55-bp deletion in exon 9 of the glucocerebrosidase gene was identified in a 28-year-old male affected with Gaucher disease. The diagnosis was established…”
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    Prenatal diagnosis in known fragile X carriers by Maddalena, A, Hicks, B D, Spence, W C, Levinson, G, Howard-Peebles, P N

    Published in American journal of medical genetics (15-07-1994)
    “…Prenatal diagnosis for fragile X syndrome was performed in 34 pregnancies of 33 known carriers, on 22 chorionic villus samples (CVS), and 15 amniocentesis…”
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    Recent Advances in Reproductive Genetic Technologies by Levinson, Gene, Coulam, Carolyn B, Spence, W. Christine, Sherins, Richard J, Schulman, Joseph D

    Published in Bio/technology (New York, N.Y. 1983) (01-09-1995)
    “…New possibilities for the diagnosis and treatment of reproductive and genetic disorders are becoming available as a result of a series of recent technical…”
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    Instrumental "-Eur/-Ateur/-Euse/-Atrice" by Spence, N. C. W.

    Published in The Modern language review (01-01-1990)
    “…The puzzle that instrumental French suffixes "-oir" and "-oire" have been almost completely replaced in modern times with "-eur/-euse," "-(a)teur" and…”
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    A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in blood by Maddalena, Anne, Yadvish, Karen N., Spence, W. Christine, Howard-Peebles, Patricia N.

    Published in American journal of medical genetics (09-08-1996)
    “…Individuals with developmental delay who are found to have only fragile X premutations present an interpretive dilemma. The presence of the premutation could…”
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    A Note on the History of the French Definite Article le/la/les by Spence, N. C. W.

    Published in Romance philology (01-02-1976)
    “…The irregularity of the phonetic development of French definite articles le, la, les from the Latin ille is noted. Parallels between the evolution of one…”
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    Psychosocial characteristics of institutionalized adolescents: Resilient or at risk? by Hutchinson, R L, Spence, W C

    Published in Adolescence (01-01-1992)
    “…The findings suggest that these adolescents may not be as psychologically dysfunctional as is commonly surmised, considering their accumulated life events,…”
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