Barth syndrome von Clarke, Sarah L N, Bowron, Ann, Gonzalez, Iris L, Groves, Sarah J, Newbury-Ecob, Ruth, Clayton, Nicol, Martin, Robin P, Tsai-Goodman, Beverly, Garratt, Vanessa, Ashworth, Michael, Bowen, Valerie M, McCurdy, Katherine R, Damin, Michaela K, Spencer, Carolyn T, Toth, Matthew J, Kelley, Richard I, Steward, Colin G

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Cardiac and Clinical Phenotype in Barth Syndrome von Spencer, Carolyn T, Bryant, Randall M, Day, Jane, Gonzalez, Iris L, Colan, Steven D, Thompson, W. Reid, Berthy, Julie, Redfearn, Sharon P, Byrne, Barry J

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Tafazzin splice variants and mutations in Barth syndrome von Kirwin, Susan M., Manolakos, Athena, Barnett, Sarah Swain, Gonzalez, Iris L.

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HRAS mutation analysis in Costello syndrome: Genotype and phenotype correlation von Gripp, Karen W., Lin, Angela E., Stabley, Deborah L., Nicholson, Linda, Scott Jr, Charles I., Doyle, Daniel, Aoki, Yoko, Matsubara, Yoichi, Zackai, Elaine H., Lapunzina, Pablo, Gonzalez-Meneses, Antonio, Holbrook, Jennifer, Agresta, Cynthia A., Gonzalez, Iris L., Sol-Church, Katia

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Barth syndrome: TAZ gene mutations, mRNAs, and evolution von Gonzalez, Iris L.

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Human rDNA: Evolutionary Patterns within the Genes and Tandem Arrays Derived from Multiple Chromosomes von Gonzalez, Iris L., Sylvester, James E.

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A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMA von Kirwin, Susan M., Vinette, Kathy M. B., Gonzalez, Iris L., Abdulwahed, Hind Al, Al‐Sannaa, Nouriya, Funanage, Vicky L.

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Multiple transmissions of Barth syndrome through an oocyte donor with a de novo TAZ mutation von Kirwin, Susan M., B.S, Vinette, Kathy M., M.S, Schwartz, Sharon B., M.S, Funanage, Vicky L., Ph.D, Gonzalez, Iris L., Ph.D

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Paternal bias in parental origin of HRAS mutations in Costello syndrome von Sol-Church, Katia, Stabley, Deborah L., Nicholson, Linda, Gonzalez, Iris L., Gripp, Karen W.

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Complete Sequence of the 43-kb Human Ribosomal DNA Repeat: Analysis of the Intergenic Spacer von Gonzalez, Iris L., Sylvester, James E.

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Studies of the Inheritance of Human Ribosomal DNA Variants Detected in Two-Dimensional Separations of Genomic Restriction Fragments von Kuick, R, Asakawa, J. I, Neel, J. V, Kodaira, M, Satoh, C, Thoraval, D, Gonzalez, I. L, Hanash, S. M

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A homozygous double mutation in SMN 1 : a complicated genetic diagnosis of SMA von Kirwin, Susan M., Vinette, Kathy M. B., Gonzalez, Iris L., Abdulwahed, Hind Al, Al‐Sannaa, Nouriya, Funanage, Vicky L.

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Effect of Triplet Repeat Expansion on Chromatin Structure and Expression of DMPK and Neighboring Genes, SIX5 and DMWD, in Myotonic Dystrophy von Frisch, Richard, Singleton, Kenneth R., Moses, Priscilla A., Gonzalez, Iris L., Carango, Paul, Marks, Harold G., Funanage, Vicky L.

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A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome von Fan, Yuxin, Steller, Jon, Gonzalez, Iris L., Kulik, Wim, Fox, Michelle, Chang, Richard, Westerfield, Brandy A., Batra, Anjan S., Wang, Raymond Yu Jeang, Gallant, Natalie M., Pena, Liana S., Wang, Hu, Huang, Taosheng, Bhuta, Sunita, Penny, Daniel J., McCabe, Edward R., Kimonis, Virginia E.

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Beyond ribosomal DNA: on towards the telomere von Gonzalez, I L, Sylvester, J E

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Cardiac and clinical phenotype in Barth syndrome.(Author abstract) von Spencer, Carolyn T, Bryant, Randall M, Day, Jane, Gonzalez, Iris L, Colan, Steven D, Thompson, W. Reid, Berthy, Julie, Redfearn, Sharon P, Byrne, Barry J

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Human Ribosomal RNA Variants from a Single Individual and Their Expression in Different Tissues von Kuo, Bruce A., Gonzalez, Iris L., Gillespie, David A., Sylvester, James E.

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The Topographic Organization of Repetitive DNA in the Human Nucleolus von Kaplan, Frederick S., Murray, John, Sylvester, James E., Gonzalez, Iris L., O'Connor, J.Patrick, Doering, Jeffrey L., Muenke, Maximilian, Emanuel, Beverly S., Zasloff, Michael A.

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Fixation Times of Retroposons in the Ribosomal DNA Spacer of Human and Other Primates von Gonzalez, Iris L., Tugendreich, Stuart, Hieter, Philip, Sylvester, James E.

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Human ribosomal RNA intergenic spacer sequence von Gonzalez, Iris L., Wu, Shuang, Li, Wen-Mei, Kuo, Bruce A., Sylvester, James E.

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