These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
117 related articles for article (PubMed ID: 6334993)
21. Hereditary multiple exostoses: confirmation of linkage to chromosomes 8 and 11. Blanton SH; Hogue D; Wagner M; Wells D; Young ID; Hecht JT Am J Med Genet; 1996 Mar; 62(2):150-9. PubMed ID: 8882395 [TBL] [Abstract][Full Text] [Related]
22. [Bessel-Hagen disease in children. Considerations of some clinical cases]. Trifan N; Dimitriu AG; Lupu V; Mardare D; Voinescu C; Petrea O Rev Med Chir Soc Med Nat Iasi; 1985; 89(2):329-31. PubMed ID: 3878987 [No Abstract] [Full Text] [Related]
23. [Hereditary multiple exostoses: a pedigree with ten cases]. Zhou YA; Ma YX; Hao ZQ; Zhang YH; Li XJ; Shi YY; Zhang QB; Li PL Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct; 29(5):613-4. PubMed ID: 23042404 [No Abstract] [Full Text] [Related]
24. Interstitial deletion of 11(p11.2p12): a newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2). Potocki L; Shaffer LG Am J Med Genet; 1996 Mar; 62(3):319-25. PubMed ID: 8882796 [TBL] [Abstract][Full Text] [Related]
25. Possible examples of the goltz syndrome (focal dermal hypoplasia) without linear areas of skin hypoplasia. Aymé S; Fraser FC Birth Defects Orig Artic Ser; 1982; 18(3B):59-65. PubMed ID: 7139115 [No Abstract] [Full Text] [Related]
26. [From gene to disease; hereditary multiple exostoses]. Wuyts W; Bovée JV; Hogendoorn PC Ned Tijdschr Geneeskd; 2002 Jan; 146(4):162-4. PubMed ID: 11845565 [TBL] [Abstract][Full Text] [Related]
33. Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly. Halal F; Picard JL; Raymond-Tremblay D; de Bosset P Am J Med Genet; 1982 Sep; 13(1):71-9. PubMed ID: 7137223 [TBL] [Abstract][Full Text] [Related]
34. A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosis. Xiao CY; Wang J; Zhang SZ; Van Hul W; Wuyts W; Qiu WM; Wu H; Zhang G Br J Cancer; 2001 Jul; 85(2):176-81. PubMed ID: 11461073 [TBL] [Abstract][Full Text] [Related]
35. [Giedion syndrome with a 46,XY karyotype in a female subject]. Resentini M; Cacopardo L; Grugni G; Morabito F Pathologica; 1986; 78(1057):657-60. PubMed ID: 3498143 [No Abstract] [Full Text] [Related]
36. Hereditary deforming dyschondroplasia. Two case report followed through four generations of each family. Pandey S Int Surg; 1970 Oct; 54(4):264-7. PubMed ID: 5311860 [No Abstract] [Full Text] [Related]
37. Osteoglophonic dwarfism in two generations. Kelley RI; Borns PF; Nichols D; Zackai EH J Med Genet; 1983 Dec; 20(6):436-40. PubMed ID: 6606709 [TBL] [Abstract][Full Text] [Related]
38. A collaborative approach to the diagnosis of a lethal short limb skeletal dysplasia. Carvalho L; Soares M; Feijóo MJ; Gaspar M; Ferreira F Genet Couns; 1997; 8(2):139-43. PubMed ID: 9219013 [TBL] [Abstract][Full Text] [Related]
39. [The Robinow syndrome: a report of a family with autosomal dominant transmission]. Díaz López MT; Lorenzo Sanz G; Quintana Castilla A; Esteve de Pablo C; Aparicio Meix JM An Esp Pediatr; 1996 May; 44(5):520-3. PubMed ID: 8928981 [No Abstract] [Full Text] [Related]
40. Cataracts, motor system disorder, short stature, learning difficulties, and skeletal abnormalities: a new syndrome? Slavotinek AM; Pike M; Mills K; Hurst JA Am J Med Genet; 1996 Mar; 62(1):42-7. PubMed ID: 8779323 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]