Prenatal diagnosis of fragile X syndrome von Hirst, Mark, Knight, Samantha, Davies, Kay, Cross, Gareth, Ocraft, Kevin, Raeburn, Sandy, Heeger, Shauna, Eunpu, Deborah, Jenkins, EdmundC, Lindenbaum, Richard, Dobkin, CarlS, Ding, Xiao-Hua, Jenkins, EdmundC, Krawczun, MichaelS, Ted Brown, W, Goonewardena, Ponmani, Willner, Judy, Benson, Cindy, Heitz, Dominique, Rousseau, Francois

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Localization of a human gene homologous to the PrP gene on the p ARM of chromosome 20 and detection of PrP-related antigens in normal human brain von Robakis, Nikolaos K., Devine-Gage, Evelyn A., Jenkins, Edmund C., Kascsak, Richard J., Brown, W.Ted, Krawczun, Michael S., Silverman, Wayne P.

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Study of spindle microtubule reassembly in cells from Alzheimer and down syndrome patients following exposure to colcemid von KRAWCZUN, M. S, JENKINS, E. C, LELE, K. P, SERSEN, E. A, WISNIEWSKI, H. M

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The Fragile X Syndrome von BROWN, W. TED, JENKINS, EDMUND C., KRAWCZUN, MICHAEL S., WISNIEWSKI, KRYSTYNA, RUDELLI, RAUL, COHEN, IRA L., FISCH, GENE, WOLF-SCHEIN, ENID, MIEZEJESKI, CHARLES, DOBKIN, CARL

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Fragile X syndrome in females with autism von Cohen, Ira L., Brown, W. Ted, Jenkins, Edmund C., Krawczun, Michael S., French, Joseph H., Raguthu, Simchalam, Wolf-Schein, Enid G., Sudhalter, Vicki, Fisch, Gene, Wisniewski, Krystyna

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The Fragile X Syndromea von BROWN, W. TED, JENKINS, EDMUND C., KRAWCZUN, MICHAEL S., WISNIEWSKI, KRYSTYNA, RUDELLI, RAUL, COHEN, IRA L., FISCH, GENE, WOLF‐SCHEIN, ENID, MIEZEJESKI, CHARLES, DOBKIN, CARL

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FRA(X)(p22) NOT ASSOCIATED WITH INFANTILE AUTISM von Fitchett, M., Jenkins, EdmundC, Brown, W.Ted, Krawczun, MichaelS, Duncan, CharlotteJ, Brooks, Judith, Gross, Ann, Lele, KusumP, Masia, Annette, Nolin, SarahL, Sanz, MaureenM, Cohen, Ira

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Patterns of BrdU incorporation in homogeneously staining regions and double minutes von Krawczun, Michael S., Camargo, Mauricio, Cervenka, Jaroslav

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Double minutes and other chromosomal aberrations in two malignant cell lines of the German cockroach Blattella germanica von Mukherjee, Asit B., Krawczun, Michael S.

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Prenatal detection of Fra(X)(q27.3) in female identical twins: Reliability of low level cytogenetic prenatal expression in females von Jenkins, Edmund C., Brown, W. Ted, Schonberg, Steven, Krawczun, Michael S., Goldberg, James, Golbus, Mitchell S.

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Fra(X) prenatal diagnosis: Are endoreduplicated and polyploid cells useful diagnostic criteria? von Krawczun, Michael S., Duncan, Charlotte J., Stark-Houck, Sandra L., Jenkins, Edmund C.

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Dialyzed fetal Bovine serum increases cytogenetic fragile X expression von Jenkins, Edmund C., Duncan, Charlotte J., Gu, Hong, Genovese, Marilyn, Krawczun, Michael S.

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Improved prenatal detection of fra(X)(q27.3): Methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures von Jenkins, Edmund C., Krawczun, Michael S., Stark-Houck, Sandra L., Duncan, Charlotte J., Kunaporn, Suphat, Gu, Hong, Schwartz-Richstein, Carol, Howard-Peebles, Patricia N., Gross, Anne, Sherman, Stephanie L., Brown, W. Ted

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Distribution of autosomal fragile sites in specimens cultured for prenatal fragile X diagnosis von Krawczun, Michael S., Jenkins, Edmund C., Duncan, Charlotte J., Stark-Houck, Sandra L., Kunaporn, Suphat, Schwartz-Richstein, Carol, Gu, Hong, Brown, W. Ted

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Fragile X expression in short-term whole blood cultures is affected by cell density von Krawczun, Michael S., Jenkins, Edmund C., Brown, W. Ted, Silverman, Wayne P.

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Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome von Jenkins, Edmund C., Genovese, Marilyn J., Duncan, Charlotte J., Gu, Hong, Stark-Houck, Sandra L., Lele, Kusum, Li, Shu-Yun, Krawczun, Michael S.

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Fragile X expression increased by low cell-culture density von Krawczun, Michael S., Lele, Kusum P., Jenkins, Edmund C., Brown, W. Ted, Opitz, John M., Reynolds, James F.

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Constitutive fragile sites in fra(X) individuals von Jenkins, Edmund C., Lele, Kusum P., Krawczun, Michael S., Gross, Anne C., Duncan, Charlotte J., Brown, W. Ted

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Recent experience in prenatal fra(X) detection von Jenkins, Edmund C., Brown, W. Ted, Krawczun, Michael S., Duncan, Charlotte J., Lele, Kusum P., Cantu, Eduardo S., Schonberg, Steven, Golbus, Mitchell S., Sekhon, Gurbax S., Stark, Sandra, Kunaporn, Suphat, Silverman, Wayne P.

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Fragile X chromosome frequency is consistent temporally and within replicate cultures von Jenkins, Edmund C., Kastin, Bruce R., Krawczun, Michael S., Lele, Kusum P., Silverman, Wayne P., Brown, W. Ted, Opitz, John M., Reynolds, James F.

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