PubMed (OMIM) for id: 10082

Year	Number of Results
1987	1
1989	1
1991	2
1994	1
1995	3
1998	1
1999	2
2001	1
2003	1
2004	1
2005	1
2007	1
2009	1
2012	1
2024	0

1

Astrocyte glypicans 4 and 6 promote formation of excitatory synapses via GluA1 AMPA receptors.

Allen NJ, Bennett ML, Foo LC, Wang GX, Chakraborty C, Smith SJ, Barres BA. Allen NJ, et al. Nature. 2012 May 27;486(7403):410-4. doi: 10.1038/nature11059. Nature. 2012. PMID: 22722203 Free PMC article.

2

Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia.

Campos-Xavier AB, Martinet D, Bateman J, Belluoccio D, Rowley L, Tan TY, Baxová A, Gustavson KH, Borochowitz ZU, Innes AM, Unger S, Beckmann JS, Mittaz L, Ballhausen D, Superti-Furga A, Savarirayan R, Bonafé L. Campos-Xavier AB, et al. Am J Hum Genet. 2009 Jun;84(6):760-70. doi: 10.1016/j.ajhg.2009.05.002. Epub 2009 May 28. Am J Hum Genet. 2009. PMID: 19481194 Free PMC article.

3

Omodysplasia: the first reported Brazilian case.

Albano LM, Oliveira LA, Bertola DR, Mazzu JF, Kim CA. Albano LM, et al. Clinics (Sao Paulo). 2007 Aug;62(4):531-4. doi: 10.1590/s1807-59322007000400023. Clinics (Sao Paulo). 2007. PMID: 17823719 Free article. No abstract available.

4

Autosomal recessive omodysplasia: early prenatal diagnosis and a possible clue to the gene location.

Tan TY, McGillivray G, Kornman L, Fink AM, Superti-Furga A, Bonafé L, Francis DI, Savarirayan R. Tan TY, et al. Am J Med Genet A. 2005 Jun 15;135(3):324-7. doi: 10.1002/ajmg.a.30754. Am J Med Genet A. 2005. PMID: 15887278

5

Recessive omodysplasia: five new cases and review of the literature.

Elçioglu NH, Gustavson KH, Wilkie AO, Yüksel-Apak M, Spranger JW. Elçioglu NH, et al. Pediatr Radiol. 2004 Jan;34(1):75-82. doi: 10.1007/s00247-003-1064-9. Epub 2003 Oct 18. Pediatr Radiol. 2004. PMID: 14566439 Review.

6

Anaesthesia in a child with autosomal recessive omodysplasia.

Di Luca BJ, Mitchell A. Di Luca BJ, et al. Anaesth Intensive Care. 2001 Feb;29(1):71-3. doi: 10.1177/0310057X0102900115. Anaesth Intensive Care. 2001. PMID: 11261917

7

Glypican-6, a new member of the glypican family of cell surface heparan sulfate proteoglycans.

Veugelers M, De Cat B, Ceulemans H, Bruystens AM, Coomans C, Dürr J, Vermeesch J, Marynen P, David G. Veugelers M, et al. J Biol Chem. 1999 Sep 17;274(38):26968-77. doi: 10.1074/jbc.274.38.26968. J Biol Chem. 1999. PMID: 10480909 Free article.

8

GPC6, a novel member of the glypican gene family, encodes a product structurally related to GPC4 and is colocalized with GPC5 on human chromosome 13.

Paine-Saunders S, Viviano BL, Saunders S. Paine-Saunders S, et al. Genomics. 1999 May 1;57(3):455-8. doi: 10.1006/geno.1999.5793. Genomics. 1999. PMID: 10329016

9

Autosomal-recessive omodysplasia: prenatal diagnosis and histomorphometric assessment of the physeal plates of the long bones.

Borochowitz Z, Sabo E, Misselevitch I, Boss JH. Borochowitz Z, et al. Am J Med Genet. 1998 Mar 19;76(3):238-44. doi: 10.1002/(sici)1096-8628(19980319)76:3<238::aid-ajmg7>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9508243

10

Nosology of omodysplasia.

Borochowitz Z, Barak M, Hershkowitz S. Borochowitz Z, et al. Am J Med Genet. 1995 Sep 25;58(4):377-8. doi: 10.1002/ajmg.1320580416. Am J Med Genet. 1995. PMID: 8533851 No abstract available.

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