Characterization of Neo-Centromeres in Marker Chromosomes Lacking Detectable Alpha-satellite DNA von Depinet, Theresa W., Zackowski, Joleen L., Earnshaw, William C., Kaffe, Sara, Sekhon, Gurbax S., Stallard, Richard, Sullivan, Beth A., Vance, Gail H., Van Dyke, Daniel L., Willard, Huntington F., Zinn, Arthur B., Schwartz, Stuart

Volltext

Recurrent immune cytopenias in two patients with DiGeorge/velocardiofacial syndrome von DePiero, Andrew D., Lourie, Eli M., Berman, Brian W., Robin, Nathaniel H., Zinn, Arthur B., Hostoffer, Robert W.

Volltext

Characterization of a familial balanced rec(13) in a child with mild MR and his half‐sibling with two structurally rearranged chromosomes 13 von Mehra, S., Christ, L., Jeng, L., Zinn, A. B., Schwartz, S.

Volltext

The need for anonymous genetic counseling and testing von MEHLMAN, M. J, KODISH, E. D, WHITEHOUSE, P, ZINN, A. B, SOLLITTO, S, BERGER, J, CHIAO, E. J, DOSICK, M. S, CASSIDY, S. B

Volltext

Inherited WT1 mutation in Denys-Drash syndrome von COPPES, M. J, LIEFERS, G. J, HIGUCHI, M, ZINN, A. B, WILLIAMSON BALFE, J, WILLIAMS, B. R. G

Volltext

Maculopathy in spinocerebellar ataxia type 7 von Morrow, M J, Zinn, A B, Tucker, T, Leigh, R J

Volltext

A 13-year-old boy with cognitive impairment, retinoblastoma, and Wilson disease von RILEY, David, WIZNITZER, Max, SCHWARTZ, Stuart, ZINN, Arthur B

Volltext

Fumarase Deficiency: A New Cause of Mitochondrial Encephalomyopathy von Zinn, Arthur B, Kerr, Douglas S, Hoppel, Charles L

Volltext

Ethylmalonic/adipic aciduria : effects of oral medium-chain triglycerides, carnitine, and glycine on urinary excretion of organic acids, acylcarnitines, and acylglycines von RINALDO, P, WELCH, R. D, PREVIS, S. F, SCHMIDT-SOMMERFELD, E, GARGUS, J. J, O'SHEA, J. J, ZINN, A. B

Volltext

Preparation of glycopeptides and oligosaccharides from thyroxine-binding globulin von Zinn, A B, Marshall, J S, Carlson, D M

Volltext

Variable expression of osteogenesis imperfecta in a nuclear family is explained by somatic mosaicism for a lethal point mutation in the αI(I) gene (COLIAI) of type I collagen in a... von WALLIS, G. A, STARMAN, B. J, ZINN, A. B, BYERS, P. H

Volltext

Delineation of the Marfan phenotype associated with mutations in exons 23-32 of the FBN1 gene von Putnam, Elizabeth A., Cho, Mimi, Zinn, Arthur B., Towbin, Jeffrey A., Byers, Peter H., Milewicz, Dianna M.

Volltext

Carbohydrate structures of thyroxine-binding globulin and their effects on hepatocyte membrane binding von Zinn, A B, Marshall, J S, Carlson, D M

Volltext

Comparison of theory and experiment for solute transport in highly heterogeneous porous medium von Golfier, F, Quintard, M, Cherblanc, F, Zinn, B.A, Wood, B.D

Volltext

Psychological response to amniocentesis: II. Effects of coping style von Phipps, Sean, Zinn, Arthur B., Opitz, John M., Reynolds, James F.

Volltext

Distal deletion of the short arm of chromosome 6 von Zurcher, Vickie L., Golden, Wendy L., Zinn, Arthur B.

Volltext

Psychological response to amniocentesis: I. Mood state and adaptation to pregnancy von Phipps, Sean, Zinn, Arthur B., Opitz, John M., Reynolds, James F.

Volltext

Sex chromosome markers: Characterization using fluorescence in situ hybridization and review of the literature von Schwartz, Stuart, Depinet, Theresa W., Leana-Cox, Julie, Isada, Nelson B., Karson, Evelyn M., Park, Vicki M., Pasztor, Linda M., Sheppard, Linda C., Stallard, Richard, Wolff, Daynna J., Zinn, Arthur B., Zurcher, Vickie L., Zackowski, Joleen L.

Volltext

Enamel defects: A developmental marker for hemifacial microsomia von Johnsen, David C., Weissman, Barbara M., Murray, Gail S., Zinn, Arthur B.

Volltext

Maternal uniparental disomy chromosome 14: Case report and literature review von Falk, Marni J., Curtis, Christine A., Bass, Nancy E., Zinn, Arthur B., Schwartz, Stuart

Volltext