Reproductive fitness in maternal homocystinuria due to cystathionine β‐synthase deficiency von Levy, H. L., Vargas, J. E., Waisbren, S. E., Kurczynski, T. W., Roeder, E. R., Schwartz, R. S., Rosengren, S., Prasad, C., Greenberg, C. R., Gilfix, B. M., MacGregor, D., Shih, V. E., Bao, L., Kraus, J. P.

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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size von Shinawi, Marwan, Liu, Pengfei, Kang, Sung-Hae L, Shen, Joseph, Belmont, John W, Scott, Daryl A, Probst, Frank J, Craigen, William J, Graham, Brett H, Pursley, Amber, Clark, Gary, Lee, Jennifer, Proud, Monica, Stocco, Amber, Rodriguez, Diana L, Kozel, Beth A, Sparagana, Steven, Roeder, Elizabeth R, McGrew, Susan G, Kurczynski, Thaddeus W, Allison, Leslie J, Amato, Stephen, Savage, Sarah, Patel, Ankita, Stankiewicz, Pawel, Beaudet, Arthur L, Cheung, Sau Wai, Lupski, James R

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Refinement of the Region for Split Hand/Foot Malformation 5 on 2q31.1 von Theisen, A., Rosenfeld, J.A., Shane, K., McBride, K.L., Atkin, J.F., Gaba, C., Hoo, J., Kurczynski, T.W., Schnur, R.E., Coffey, L.B., Zackai, E.H., Schimmenti, L., Friedman, N., Zabukovec, M., Ball, S., Pagon, R., Lucas, A., Brasington, C.K., Spence, J.E., Sparks, S., Banks, V., Smith, W., Friedberg, T., Wyatt, P.R., Aust, M., Tervo, R., Crowley, A., Skidmore, D., Lamb, A.N., Ravnan, B., Sahoo, T., Schultz, R., Torchia, B.S., Sgro, M., Chitayat, D., Shaffer, L.G.

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Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food von Yannicelli, Steven, Acosta, Phyllis B, Velazquez, Antonio, Bock, Hans-Georg, Marriage, Barbara, Kurczynski, Thaddeus W, Miller, Marvin, Korson, Mark, Steiner, Robert D, Rutledge, Lane, Bernstein, Laurie, Chinsky, Jeffrey, Galvin-Parton, Patricia, Arnold, Georgianne L

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Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3 von Nesslinger, N J, Gorski, J L, Kurczynski, T W, Shapira, S K, Siegel-Bartelt, J, Dumanski, J P, Cullen, Jr, R F, French, B N, McDermid, H E

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Neonatal Encephalopathy in Two Boys in Families With Recurrent Rett Syndrome von Schanen, N. Carolyn, Kurczynski, Thaddeus W., Brunelle, David, Woodcock, Maureen M., Dure, Leon S., Percy, Alan K.

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Auralcephalosyndactyly: a new hereditary craniosynostosis syndrome von Kurczynski, T W, Casperson, S M

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Metabolic studies of carnitine in a child with propionic acidemia von KURCZYNSKI, T. W, HOPPEL, C. L, GOLDBLATT, P. J, GUNNING, W. T

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Hereditary cutis marmorata telangiectatica congenita von Kurczynski, T W

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Evaluation of the Health Belief Model and Decision Making Regarding Amniocentesis in Women of Advanced Maternal Age von French, Beatrice N., Kurczynski, Thaddeus W., Weaver, Michael T., Pituch, Martha J.

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Long-term l-carnitine treatment in isovaleric acidemia von Mayatepek, Ertan, Kurczynski, Thaddeus W., Hoppel, Charles L.

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Head-upright tilt table testing in evaluation of recurrent, unexplained syncope von Grubb, Blair P., Orecchio, Edward, Kurczynski, Thaddeus W.

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ANTENATAL DIAGNOSIS OF PENA-SHOKEIR SYNDROME (TYPE I) WITH ULTRASONOGRAPHY AND MAGNETIC RESONANCE IMAGING von Persutte, Wayne H, Lenke, Roger R, Kurczynski, Thaddeus W, Brinker, Ray A

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Carnitine deficiency associated with ornithine transcarbamylase deficiency von Mayatepek, Ertan, Kurczynski, Thaddeus W., Hoppel, Charles L., Gunning, William T.

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Autosomal recessive neurodegenerative disorder with trichorrhexis invaginata and ectodermal dysplasia von Gyure, Kymberly A., Kurczynski, Thaddeus W., Gunning, William, French, Beatrice N.

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Studies of a family with incontinentia pigmenti variably expressed in both sexes von Kurczynski, T W, Berns, J S, Johnson, W E

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Prenatal diagnosis of autosomal dominant microcephaly and postnatal evaluation with magnetic resonance imaging von Persutte, Wayne H., Kurczynski, Thaddeus W., Chaudhuri, K., Lenke, Roger R., Woldenberg, Lee, Brinker, Ray A.

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New marfanoid syndrome with craniosynostosis von Furlong, Judith, Kurczynski, Thaddeus W., Hennessy, James R., Reynolds, James F.

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A general program for maximum likelihood estimation of gene frequencies von Kurczynski, T W, Steinberg, A G

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Unilateral Retinoblastoma with Acquired Monosomy 7 and Secondary Acute Myelomonocytic Leukemia von Bayar, Emel, Robinson, Margaret G., Kurczynski, Thaddeus W.

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