Hereditary multiple exostoses: Confirmation of linkage to chromosomes 8 and 11

American Journal of Medical Genetics

Volumn 62, Issue 2, 1996, Pages 150-159

  Blanton, Susan Halloran ^a   Hogue, Deborah ^b   Wagner, Michael ^c   Wells, Dan ^c   Young, Ian D ^d   Hecht, Jacqueline T ^b  

^a UNIVERSITY OF VIRGINIA   (United States)

^b UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^c University of Houston ^*  (United States)

^d NOTTINGHAM CITY HOSPITAL   (United Kingdom)

Author keywords

chromosome 11; chromosome 19; chromosome 8; EXT; genetic study; haplotype; hereditary multiple exostoses; Lager Giedion syndrome; linkage study

Indexed keywords

ARTICLE; CHROMOSOME 11; CHROMOSOME 19; CHROMOSOME 8; CHROMOSOME MAP; CLINICAL ARTICLE; FAMILY STUDY; GENE LOCUS; GENETIC LINKAGE; HEREDITARY MULTIPLE EXOSTOSIS; HUMAN; PEDIGREE; PRIORITY JOURNAL;

EID: 0030006019     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1096-8628(19960315)62:2<150::aid-ajmg7>3.0.co;2-%23     Document Type: Article

References (19)

1. Buhler EM, Malik NJ (1984): The tricho-rhino-phalangeal syndrome(s): Chromosome 8 deletion: is there a shortest region of overlap between reported cases? TRPI and TRPII syndromes: Are they separate entities? Am J Med Genet 19:113-119.
2. Cook A, Raskind W, Blanton SH, Pauli RM, Gregg RG, Francomano CA, Puffenberger E, Conrad EU, Schmale G, Schallenberg G, Wijsman E, Hecht JT, Wells D, Wagner MJ (1993): Genetic heterogeneity in families with hereditary multiple exostoses. Am J Hum Genet 53:71-79.
3. Cottingham RW, Idury RM, Schaffer AA (1993): Faster sequential genetic linkage computations. Am J Hum Genet 53:252-263.
4. Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bernardi G, Lathrop M, Weissenbach J (1994): The 1993-94 Genethon human genetic linkage map. Nature Genet 7:246-266.
5. Hecht JT, Wang Y, Connor B, Blanton SH, Daiger SP (1993): Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A. Am J Human Genet 52:1230-1233.
6. Hecht JT, Hogue D, Strong LC, Hansen M, Blanton SH, Wagner MJ (1995): Hereditary multiple exostoses and chondrosarcoma: Linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosomes 11 and 8. Am J Hum Genet 56:1125-1131.
7. Lathrop GM, Lallouel JM, Julier C, Ott J (1984): Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci USA 81: 3443-3446.
8. Le Merrer M, Legeal-Mallet L, Jeannin PM, Horsthemke B, Schinzel A, Plauchu H, Toutain A, Achard F, Munnich A, Maroteaux P (1994): A gene for hereditary multiple exostoses maps to chromosome 19p. Hum Mol Genet 3:717-722.
9. Luckert-Wicklund C, Pauli RM, Johnston D, Hecht JT (1995): Natural history study of hereditary multiple exostoses. Am J Hum Genet 55:43-46.
10. Ludecke H-J, Wagner MJ, Nardmann J, La Pillo B, Parrish JE, Willems PJ, Haan EA, Frydman M, Hammers GJH, Wells DE, Horsthemke B (1995): Molecular dissection of a contiguous gene syndrome localization of the genes involved in the Langer-Giedion syndrome. Hum Mol Genet 4:31-36.
11. Mertens F, Rydholm A, Kreiebergs A, Eillen H, Jonsson K, Heim S, Mitelman F, Mandahl N (1994): Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses. Genes Chromosomes Cancer 9:8-12.
12. Ogle RF, Dalzell P, Turner G, Wass D, Yip M-Y (1991): Multiple exostoses in a patient with t(8;11)(q24.11;p15.5). J Med Genet 28:881-683.
13. Ott J (1991): "Analysis of Human Genetic Linkage." Baltimore: Johns Hopkins University Press.
14. Sambrook J, Fritsch F, Maniatis T (1989): "Molecular Cloning: A Laboratory Manual," 2nd ED. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
15. Schmale GA, Conrad EU, Raskind WH (1994): The natural history of hereditary multiple exostoses. J Bone Jt Surg 76A:986-992.
16. Solomon L (1963): Hereditary multiple exostosis. J Bone Jt Surg 458:292-304.
17. Tomfohrde J, Wood S, Schertzer M, Wagner MJ, Wells DE, Parish J, Sadler LA, Blanton SH, Daiger SP, Wang Z, Wilkie PJ, Weber JL (1992): Human chromosome 8 linkage MAP based on short tandem repeat polymorphisms: Effect of genotyping errors. Genomics 14:144-152.
18. Wu Y-Q, Heutink P, de Vries BBA, Sandkuijl LA, van den Ouweland AMW, Niermeijer MF, Galjaard H, Reyniers E, Willems PJ, Halley DJJ (1994): Assignment of a second locus for multiple exostoses to the pericentric region of chromosome 11. Hum Mol Genet 3:167-171.
19. Yoshiura K, Inazawa J, Koyama K, Nakamura Y, Niikawa N (1994): Mapping of the 8q23 translocation breakpoint of t(8;13) observed in a patient with multiple exostoses. Genes Chromosomes Cancer 9:57-61.