PMC Links for OMIM (Select 133701) - PMC

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Items: 7

Select item 18015601.

Refinement of the Multiple Exostoses Locus (EXT2) to a 3-cM Interval on Chromosome 11

Wim Wuyts, Sarvan Ramlakhan, Wim Van Hul, Jacqueline T. Hecht, Ans M. W. van den Ouweland, Wendy H. Raskind, Floris C. Hofstede, Edwin Reyniers, Dan E. Wells, Bert de Vries, Ernest U. Conrad, April Hill, Dmitry Zalatayev, Jean Weissenbach, Michael J. Wagner, Egbert Bakker, Dicky J. J. Halley, Patrick J. Willems

Am J Hum Genet. 1995 Aug; 57(2): 382–387.

PMCID:: PMC1801560

Summary Page Browse PDF–1.0M

Select item 18014502.

Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8.

J T Hecht, D Hogue, L C Strong, M F Hansen, S H Blanton, M Wagner

Am J Hum Genet. 1995 May; 56(5): 1125–1131.

PMCID:: PMC1801450

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Select item 17571863.

Genotype-phenotype correlation in hereditary multiple exostoses

C Francannet, A Cohen-Tanugi, M Le Merrer, A Munnich, J Bonaventure, L Legeai-Mallet

J Med Genet. 2001 Jul; 38(7): 430–434. doi: 10.1136/jmg.38.7.430

PMCID:: PMC1757186

Summary PDF–118K

Select item 17159394.

Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses.

C Philippe, D E Porter, M E Emerton, D E Wells, A H Simpson, A P Monaco

Am J Hum Genet. 1997 Sep; 61(3): 520–528. doi: 10.1086/515505

PMCID:: PMC1715939

Summary Page Browse PDF–1.3M

Select item 16822315.

Genetic heterogeneity in families with hereditary multiple exostoses

April Cook, Wendy Raskind, Susan Halloran Blanton, Richard M. Pauli, Ronald G. Gregg, Claire A. Francomano, Eric Puffenberger, Ernest U. Conrad, Gregory Schmale, Gerard Schellenberg, Ellen Wijsman, Jacqueline T. Hecht, Dan Wells, Michael J. Wagner

Am J Hum Genet. 1993 Jul; 53(1): 71–79.

PMCID:: PMC1682231

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Select item 13769016.

Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses.

W Wuyts, W Van Hul, K De Boulle, J Hendrickx, E Bakker, F Vanhoenacker, F Mollica, H J Lüdecke, B S Sayli, U E Pazzaglia, G Mortier, B Hamel, E U Conrad, M Matsushita, W H Raskind, P J Willems

Am J Hum Genet. 1998 Feb; 62(2): 346–354. doi: 10.1086/301726