Is myoglobin useful in the diagnosis of acute myocardial infarction in the emergency department setting ? von WOO, J, LACBAWAN, F. L, SUNHEIMER, R, LEFEVER, D, MCCABE, J. B

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Central nervous system embryogenesis and its failures von Lacbawan, Felicitas L, Muenke, Maximilian

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Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin von Lacbawan, Felicitas L., White, Beverly J., Anguiano, Arturo, Rigdon, David T., Ball, Karen D., Bromage, Gail B., Yang, Xiaojing, DiFazio, Marc P., Levin, Sondra W.

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A rare interstitial deletion (2)(pi l.2pl3) in a child with pericentric inversion (2)(pl l.2g13) of paternal origin von White, B. J., Lacbawan, F. L., Anguiano, A., Rigdon, D, Ball, K., Bromage, G., Yang, X. J., DiFazio, M., Levin, S. W., Diagnostics, Quest, Capistrano, San Juan, H, N I

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Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta von Cabral, Wayne A, Ishikawa, Masaki, Garten, Matthias, Makareeva, Elena N, Sargent, Brandi M, Weis, MaryAnn, Barnes, Aileen M, Webb, Emma A, Shaw, Nicholas J, Ala-Kokko, Leena, Lacbawan, Felicitas L, Högler, Wolfgang, Leikin, Sergey, Blank, Paul S, Zimmerberg, Joshua, Eyre, David R, Yamada, Yoshihiko, Marini, Joan C

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Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of BRCA1 and BRCA2 Mutation Carriers Through Family-Based Outreach von Samimi, Goli, Bernardini, Marcus Q, Brody, Lawrence C, Caga-Anan, Charlisse F, Campbell, Ian G, Chenevix-Trench, Georgia, Couch, Fergus J, Dean, Michael, de Hullu, Joanne A, Domchek, Susan M, Drapkin, Ronny, Spencer Feigelson, Heather, Friedlander, Michael, Gaudet, Mia M, Harmsen, Marline G, Hurley, Karen, James, Paul A, Kwon, Janice S, Lacbawan, Felicitas, Lheureux, Stephanie, Mai, Phuong L, Mechanic, Leah E, Minasian, Lori M, Myers, Evan R, Robson, Mark E, Ramus, Susan J, Rezende, Lisa F, Shaw, Patricia A, Slavin, Thomas P, Swisher, Elizabeth M, Takenaka, Masataka, Bowtell, David D, Sherman, Mark E

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Association between conformational mutations in neuroserpin and onset and severity of dementia von Davis, Richard L, Shrimpton, Antony E, Carrell, Robin W, Lomas, David A, Gerhard, Lieselotte, Baumann, Bruno, Lawrence, Daniel A, Yepes, Manuel, Kim, Tai Seung, Ghetti, Bernardino, Piccardo, Pedro, Takao, Masaki, Lacbawan, Felicitas, Muenke, Maximilian, Sifers, Richard N, Bradshaw, Charles B, Kent, Paul F, Collins, George H, Larocca, Daria, Holohan, Peter D

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Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function von Lacbawan, F, Solomon, B D, Roessler, E, El-Jaick, K, Domené, S, Vélez, J I, Zhou, N, Hadley, D, Balog, J Z, Long, R, Fryer, A, Smith, W, Omar, S, McLean, S D, Clarkson, K, Lichty, A, Clegg, N J, Delgado, M R, Levey, E, Stashinko, E, Potocki, L, VanAllen, M I, Clayton-Smith, J, Donnai, D, Bianchi, D W, Juliusson, P B, Njølstad, P R, Brunner, H G, Carey, J C, Hehr, U, Müsebeck, J, Wieacker, P F, Postra, A, Hennekam, R C M, van den Boogaard, M-J H, van Haeringen, A, Paulussen, A, Herbergs, J, Schrander-Stumpel, C T R M, Janecke, A R, Chitayat, D, Hahn, J, McDonald-McGinn, D M, Zackai, E H, Dobyns, W B, Muenke, M

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Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype von Bendavid, C, Haddad, B R, Griffin, A, Huizing, M, Dubourg, C, Gicquel, I, Cavalli, L R, Pasquier, L, Shanske, A L, Long, R, Ouspenskaia, M, Odent, S, Lacbawan, F, David, V, Muenke, M

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Pulmonary Dysfunction in Adults With Nephropathic Cystinosis von Anikster, Yair, Lacbawan, Felicitas, Brantly, Mark, Gochuico, Bernadette L., Avila, Nilo A., Travis, William, Gahl, William A.

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Familial Encephalopathy with Neuroserpin Inclusion Bodies von Davis, Richard L., Holohan, Peter D., Shrimpton, Antony E., Tatum, Arthur H., Daucher, John, Collins, George H., Todd, Robert, Bradshaw, Charles, Kent, Paul, Feiglin, David, Rosenbaum, Arthur, Yerby, Mark S., Shaw, Cheng-Mei, Lacbawan, Felicitas, Lawrence, Daniel A.

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TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype von Keaton, A.A., Solomon, B.D., Kauvar, E.F., El-Jaick, K.B., Gropman, A.L., Zafer, Y., Meck, J.M., Bale, S.J., Grange, D.K., Haddad, B.R., Gowans, G.C., Clegg, N.J., Delgado, M.R., Hahn, J.S., Pineda-Alvarez, D.E., Lacbawan, F., Vélez, J.I., Roessler, E., Muenke, M.

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Familial dementia caused by polymerization of mutant neuroserpin von Gooptu, Bibek, Sonderegger, Peter, Lacbawan, Felicitas, Lawrence, Daniel A, Davis, Richard L, Becker, Lyn Marie, Yerby, Mark S, Krasnewich, Donna, Holohan, Peter D, Collins, George H, Shaw, Cheng-Mei, Muenke, Maximilian, Kinter, Jochen, Elliott, Peter R, Feiglin, David, Lomas, David A, Shrimpton, Antony E, Finch, John T, Carrell, Robin W, Bradshaw, Charles

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Clinical Heterogeneity in Mitochondrial DNA Deletion Disorders: A Diagnostic Challenge of Pearson Syndrome von Lacbawan, Felicitas, Tifft, Cynthia J., Luban, Naomi L.C., Schmandt, Susanne M., Guerrera, Michael, Weinstein, Steven, Pennybacker, Mark, Wong, Lee-Jun C.

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