Low expression of Abelson interactor-1 is linked to acquired drug resistance in Bcr-Abl-induced leukemia von Chorzalska, A, Salloum, I, Shafqat, H, Khan, S, Marjon, P, Treaba, D, Schorl, C, Morgan, J, Bryke, C R, Falanga, V, Zhao, T C, Reagan, J, Winer, E, Olszewski, A J, Al-Homsi, A S, Kouttab, N, Dubielecka, P M

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Desbuquois syndrome in three sisters with significantly different lengths of survival von Lloyd, A.R., Ragosta, K.G., Bryke, C.R., Hoo, J.J.

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Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes von LINDGREN, V, CHIH-PING CHEN, BRYKE, C. R, LICHTER, P, PAGE, D. C, YANG-FENG, T. L

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Distinct Missense Mutations of the FGFR3 Lys650 Codon Modulate Receptor Kinase Activation and the Severity of the Skeletal Dysplasia Phenotype von Bellus, Gary A., Spector, Elaine B., Speiser, Phyllis W., Weaver, Christine A., Garber, Anthony T., Bryke, Christine R., Israel, Jamie, Rosengren, Sally S., Webster, Melanie K., Donoghue, Daniel J., Francomano, Clair A.

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Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis von LINDGREN, V, BRYKE, C. R, OZCELIK, T, YANG-FENG, T. L, FRANCKE, U

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Pediatric residencies: differences between 1959/1960 and 1984/1985 von BRYKE, C. R, TUNNESSEN, W. W. JR, SCULLY, T. J, OSKI, F. A

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Small cell lung cancer cell line derived from a primary tumor with a characteristic deletion of 3p von GRAZIANO, S. L, COWAN, B. Y, POIESZ, B. J, CARNEY, D. N, BRYKE, C. R, MITTER, N. S, JOHNSON, B. E, MARK, G. E, PLANAS, A. T, CATINO, J. J, COMIS, R. L

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Desbuquois syndrome: Clinical, radiographic, and morphologic characterization von Shohat, Mordechai, Lachman, Ralph, Gruber, Helen E., Hsia, Y. Edward, Golbus, Mitchell S., Witt, David R., Bodell, Adria, Bryke, Christine R., Hogge, W. Allen, Rimoin, David L.

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Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46, XY/46,XY, -18,+ dic(18)(q12.2)] von Bryke, Christine R., Lindgren, Valerie, Fryburg, Julie S., Yang-Feng, Teresa L.

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Duplication of euchromatin without phenotypic effects: A variant of chromosome 16 von Bryke, Christine R., Breg, W. Roy, Potluri, Venkateswara R., Yang-Feng, Teresa L.

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Antenatal diagnosis of 45,X/48,XYYY von Bryke, Christine R., Mahoney, Maurice J., Yang-Feng, Teresa L.

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Solitary Rectal Ulcer Syndrome in a Teenaged Boy von Sondheimer, Judith M., Slagle, Terri A., Bryke, Christine R., Hill, Rolla B.

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Remarks on constitutional 5q deletions von Rivera, H

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Desbuquois syndrome in three sisters with significantly different lengths of survival von Lloyd, A R, Ragosta, K G, Bryke, C R, Hoo, J J

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Solitary Rectal Ulcer Syndrome in a Teenaged Boy von Sondheimer, Judith M., Slagle, Terri A., Bryke, Christine R., Hill, Rolla B.

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Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas von Dai, Zunyan, Kelly, Joann C, Meloni-Ehrig, Aurelia, Slovak, Marilyn L, Boles, Debra, Christacos, Nicole C, Bryke, Christine R, Schonberg, Steven A, Otani-Rosa, Jennifer, Pan, Qiulu, Ho, Albert K, Sanders, Heather R, Zhang, Zhong J, Jones, Dan, Mowrey, Philip N

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