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Items: 1 to 20 of 33

1.

Bone growth in diaphysial aclasis.

SOLOMON L.

J Bone Joint Surg Br. 1961 Nov;43-B:700-16. No abstract available.

2.

Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family.

Wise CA, Clines GA, Massa H, Trask BJ, Lovett M.

Genome Res. 1997 Jan;7(1):10-6.

3.

Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies.

Hecht JT, Hogue D, Wang Y, Blanton SH, Wagner M, Strong LC, Raskind W, Hansen MF, Wells D.

Am J Hum Genet. 1997 Jan;60(1):80-6.

4.

Positional cloning of a gene involved in hereditary multiple exostoses.

Wuyts W, Van Hul W, Wauters J, Nemtsova M, Reyniers E, Van Hul EV, De Boulle K, de Vries BB, Hendrickx J, Herrygers I, Bossuyt P, Balemans W, Fransen E, Vits L, Coucke P, Nowak NJ, Shows TB, Mallet L, van den Ouweland AM, McGaughran J, Halley DJ, Willems PJ.

Hum Mol Genet. 1996 Oct;5(10):1547-57.

PMID:
8894688
5.

Encyclopedia of the mouse genome V. Mouse chromosome 2.

Siracusa LD, Morgan JL, Fisher JK, Abbott CM, Peters J.

Mamm Genome. 1996;6 Spec No:S51-63. No abstract available.

PMID:
8800778
6.

The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes.

Stickens D, Clines G, Burbee D, Ramos P, Thomas S, Hogue D, Hecht JT, Lovett M, Evans GA.

Nat Genet. 1996 Sep;14(1):25-32.

PMID:
8782816
7.

Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

Bartsch O, Wuyts W, Van Hul W, Hecht JT, Meinecke P, Hogue D, Werner W, Zabel B, Hinkel GK, Powell CM, Shaffer LG, Willems PJ.

Am J Hum Genet. 1996 Apr;58(4):734-42.

8.

Deletion mapping on chromosome 1p in well-differentiated gastric cancer.

Ezaki T, Yanagisawa A, Ohta K, Aiso S, Watanabe M, Hibi T, Kato Y, Nakajima T, Ariyama T, Inazawa J, Nakamura Y, Horii A.

Br J Cancer. 1996 Feb;73(4):424-8.

9.

Deletion of 1p loci and microsatellite instability in colorectal polyps.

Lothe RA, Andersen SN, Hofstad B, Meling GI, Peltomäki P, Heim S, Brøgger A, Vatn M, Rognum TO, Børresen AL.

Genes Chromosomes Cancer. 1995 Nov;14(3):182-8.

PMID:
8589034
10.

Genomic DNA sequencing methods.

Favello A, Hillier L, Wilson RK.

Methods Cell Biol. 1995;48:551-69. Review.

PMID:
8531742
11.

Genetic heterogeneity in families with hereditary multiple exostoses.

Cook A, Raskind W, Blanton SH, Pauli RM, Gregg RG, Francomano CA, Puffenberger E, Conrad EU, Schmale G, Schellenberg G, et al.

Am J Hum Genet. 1993 Jul;53(1):71-9.

12.

Effective amplification of long targets from cloned inserts and human genomic DNA.

Cheng S, Fockler C, Barnes WM, Higuchi R.

Proc Natl Acad Sci U S A. 1994 Jun 7;91(12):5695-9.

13.

Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11.

Wu YQ, Heutink P, de Vries BB, Sandkuijl LA, van den Ouweland AM, Niermeijer MF, Galjaard H, Reyniers E, Willems PJ, Halley DJ.

Hum Mol Genet. 1994 Jan;3(1):167-71.

PMID:
8162019
14.
15.

A gene for hereditary multiple exostoses maps to chromosome 19p.

Le Merrer M, Legeai-Mallet L, Jeannin PM, Horsthemke B, Schinzel A, Plauchu H, Toutain A, Achard F, Munnich A, Maroteaux P.

Hum Mol Genet. 1994 May;3(5):717-22.

PMID:
8081357
16.

Maps from two interspecific backcross DNA panels available as a community genetic mapping resource.

Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MS, Thurston SJ, Birkenmeier EH.

Mamm Genome. 1994 May;5(5):253-74. Erratum in: Mamm Genome 1994 Jul;5(7):463.

PMID:
8075499
17.

The natural history of hereditary multiple exostoses.

Schmale GA, Conrad EU 3rd, Raskind WH.

J Bone Joint Surg Am. 1994 Jul;76(7):986-92.

PMID:
8027127
18.
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20.

Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer.

Nagai H, Negrini M, Carter SL, Gillum DR, Rosenberg AL, Schwartz GF, Croce CM.

Cancer Res. 1995 Apr 15;55(8):1752-7.

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