Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations von Wijetunge, U. Kalpani S., Sirisena, Nirmala D., de Silva, Ramya, Dissanayake, Vajira H. W.

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High-density multiplex detection of nucleic acid sequences: oligonucleotide ligation assay and sequence-coded separation von Grossman, Paul D., Bloch, Will, Brinson, Eleanor, Chang, Conway C., Eggerding, Faye A., Fung, Steven, lovannisci, David A., Woo, Sam, Winn-Deen, Emily S.

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Delineation of 2q32q35 Deletion Phenotypes : Two Apparent “Proximal” and “Distal” Syndromes von Mc Cormack, Adrian, Taylor, Juliet, Gregersen, Nerine, George, Alice M., Love, Donald R.

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Introduction to PCR/OLA/SCS, a multiplex DNA test, and its application to cystic fibrosis von Brinson, E C, Adriano, T, Bloch, W, Brown, C L, Chang, C C, Chen, J, Eggerding, F A, Grossman, P D, Iovannisci, D M, Madonik, A M, Sherman, D G, Tam, R W, Winn-Deen, E S, Woo, S L, Fung, S, Iovannisci, D A

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Maternal Smoking and the Risk of Orofacial Clefts: Susceptibility with NAT1 and NAT2 Polymorphisms von Lammer, Edward J., Shaw, Gary M., Iovannisci, David M., Van Waes, Janee, Finnell, Richard H.

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Maternal Smoking, Genetic Variation of Glutathione S-Transferases, and Risk for Orofacial Clefts von Lammer, Edward J., Shaw, Gary M., Iovannisci, David M., Finnell, Richard H.

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Genetic polymorphisms and cerebral palsy in very preterm infants von Nelson, Karin B, Dambrosia, James M, Iovannisci, David M, Cheng, Suzanne, Grether, Judith K, Lammer, Edward

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Endothelial Nitric Oxide Synthase (NOS3) Genetic Variants, Maternal Smoking, Vitamin Use, and Risk of Human Orofacial Clefts von Shaw, Gary M., Iovannisci, David M., Yang, Wei, Finnell, Richard H., Carmichael, Suzan L., Cheng, Suzanne, Lammer, Edward J.

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Maternal Occupational Chemical Exposures and Biotransformation Genotypes as Risk Factors for Selected Congenital Anomalies von Shaw, Gary M., Nelson, Verne, Iovannisci, David M., Finnell, Richard H., Lammer, Edward J.

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Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes von Shaw, Gary M., Iovannisci, David M., Yang, Wei, Finnell, Richard H., Carmichael, Suzan L., Cheng, Suzanne, Lammer, Edward J.

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Periconceptional multivitamin intake during early pregnancy, genetic variation of acetyl-N-transferase 1 (NAT1), and risk for orofacial clefts von Lammer, Edward J., Shaw, Gary M., Iovannisci, David M., Finnell, Richard H.

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Targeting nanodisks via a single chain variable antibody – Apolipoprotein chimera von Iovannisci, David M., Beckstead, Jennifer A., Ryan, Robert O.

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Structural alterations of chromosome 2 in Leishmania major as evidence for diploidy, including spontaneous amplification of the mini-exon array von Iovannisci, David M., Beverley, Stephen M.

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Fluorescence-based oligonucleotide ligation assay for analysis of cystic fibrosis transmembrane conductance regulator gene mutations von Eggerding, Faye A., Iovannisci, David M., Brinson, Eleanor, Grossman, Paul, Winn-Deen, Emily S.

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GENETIC VARIANTS AND GASTROSCHISIS: 307 von Muiru, A., Iovannisci, D. M., Shaw, G. M., Lammer, E. J.

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Genetic analysis of adenine metabolism in Leishmania donovani promastigotes. Evidence for diploidy at the adenine phosphoribosyltransferase locus von Iovannisci, D M, Goebel, D, Allen, K, Kaur, K, Ullman, B

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High efficiency plating method for Leishmania promastigotes in semidefined or completely-defined medium von Iovannisci, D.M, Ullman, B

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Ligation amplification and fluorescence detection of Mycobacterium tuberculosis DNA von Iovannisci, David M., Winn-Deen, Emily S.

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Characterization of a mutant Leishmania donovani deficient in adenosine kinase activity von Iovannisci, David M., Ullman, Buddy

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Genetic analysis of nucleoside transport in Leishmania donovani von Iovannisci, D M, Kaur, K, Young, L, Ullman, B

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