Transcriptional regulatory network analysis of developing human erythroid progenitors reveals patterns of coregulation and potential transcriptional regulators von Keller, M. A, Addya, S, Vadigepalli, R, Banini, B, Delgrosso, K, Huang, H, Surrey, S

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Organization of the gene for platelet glycoprotein IIb von Heidenreich, Randy, Eisman, Robin, Surrey, Saul, Delgrosso, Kathleen, Bennett, Joel S, Schwartz, Elias, Poncz, Mortimer

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53 EARLY EXPOSURE TO BUTYRATE INCREASES FETAL HEMOGLOBIN DURING ADULT ERYTHROID DEVELOPMENT IN VITRO von Banini, B. A., Addya, S., Delgrosso, K., Keller, M. A., Surrey, S.

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Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans von Zelante, Leopoldo, Gasparini, Paolo, Estivill, Xavier, Melchionda, Salvatore, D'Agruma, Leonardo, Govea, Nancy, Milá, Monserrat, Della Monica, Matteo, Lutfi, Jaber, Shohat, Mordechai, Mansfield, Elaine, Delgrosso, Kathleen, Rappaport, Eric, Surrey, Saul, Fortina, Paolo

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Erythroid-induced commitment of K562 cells results in clusters of differentially expressed genes enriched for specific transcription regulatory elements von Addya, Sankar, Keller, Margaret A, Delgrosso, Kathleen, Ponte, Christine M, Vadigepalli, Rajanikanth, Gonye, Gregory E, Surrey, Saul

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Identification of the Nucleotide Change (CAC→CGC) Responsible for Hb P-Galveston [β117(G19)His→Arg] von Keller, M. A., Delgrosso, K., Surrey, S., Schwartz, E.

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Early Exposure to Butyrate Increases Fetal Hemoglobin during Adult Erythroid Development in Vitro von Banini, B.A., Addya, S., Delgrosso, K., Keller, M.A., Surrey, S.

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Identification of APC gene mutations in colorectal cancer using universal microarray‐based combinatorial sequencing‐by‐hybridization von Cowie, Shannon, Drmanac, Snezana, Swanson, Donald, Delgrosso, Kathleen, Huang, Steve, du Sart, Desirée, Drmanac, Radoje, Surrey, Saul, Fortina, Paolo

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A > 200 kb deletion removing the entire β-like globin gene cluster in a family of Irish Descent von Fortina, P., Delgrosso, K., Werner, E., Haines, K., Rappaport, E., Schwartz, E., Surrey, S.

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Detection of a novel DNA polymorphism in the beta-globin gene cluster von Semenza, G L, Malladi, P, Surrey, S, Delgrosso, K, Poncz, M, Schwartz, E

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Functional analysis of a beta-globin gene containing a TATA box mutation from a Kurdish Jew with beta thalassemia von Surrey, S, Delgrosso, K, Malladi, P, Schwartz, E

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Simple two-color array-based approach for mutation detection von Fortina, P, Delgrosso, K, Sakazume, T, Santacroce, R, Moutereau, S, Su, H J, Graves, D, McKenzie, S, Surrey, S

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Interpretation of fetal hemoglobin only on Newborn screening for hemoglobinopathy von HEENEY, Matthew M, DELGROSSO, Kathleen, ROBINSON, Robbi, JOHNSON, Christine A, DAESCHNER, Charles W, CAMPBELL, Thomas A, SURREY, Saul, WARE, Russell E

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A Single-Base Change at Position - 175 in the 5’-Flanking Region of the Gγ-Globin Gene From a Black With Gγ-β+HPFH von Saul, Surrey, Kathleen, Delgrosso, Padmini, Malladi, Elias, Schwartz

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Interaction of a rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of α thalassemia von FORTINA, P, PARRELLA, T, SURREY, S, SARTORE, M, GOTTARDI, E, GABUTTI, V, DELGROSSO, K, MANSFIELD, E, RAPPAPORT, E, SCHWARTZ, E, CAMASCHELLA, C

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Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia von Fortina, P, Parrella, T, Sartore, M, Gottardi, E, Gabutti, V, Delgrosso, K, Mansfield, E, Rappaport, E, Schwartz, E, Camaschella, C

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The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions von Semenza, Gregg L., Delgrosso, Kathleen, Poncz, Mortimer, Malladi, Padmini, Schwartz, Elias, Surrey, Saul

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The – 175T → C Mutation Increases Promoter Strength in Erythroid Cells: Correlation With Evolutionary Conservation of Binding Sites for Two Trans-Acting Factors von Gumucio, Deborah L., Lockwood, Wendy K., Weber, Janice L., Saulino, Ann M., Delgrosso, Kathleen, Surrey, Saul, Schwartz, Elias, Goodman, Morris, Collins, Francis S.

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A large deletion encompassing the entire α-like globin gene cluster in a family of Northern European extraction von FORTINA, P, DELGROSSO, K, RAPPAPORT, E, PONEZ, M, BALLAS, S. K, SCHWARTZ, E, SURREY, S

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A single-base change at position -175 in the 5'-flanking region of the G gamma-globin gene from a black with G gamma-beta+ HPFH von Surrey, S, Delgrosso, K, Malladi, P, Schwartz, E

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