Similar articles for PMID: 11169564

Year	Number of Results
1908	1
1989	2
1990	1
1992	1
1993	2
1994	5
1995	3
1996	3
1997	4
1998	6
1999	3
2000	2
2001	4
2002	6
2003	4
2004	6
2005	5
2006	4
2008	4
2009	3
2010	6
2011	3
2012	3
2013	3
2014	1
2017	1
2018	4
2019	1
2020	1
2024	0

1

Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity alone.

Galjaard RJ, van der Ham LI, Posch NA, Dijkstra PF, Oostra BA, Hovius SE, Timmenga EJ, Sonneveld GJ, Hoogeboom AJ, Heutink P. Galjaard RJ, et al. Am J Med Genet. 2001 Jan 22;98(3):256-62. doi: 10.1002/1096-8628(20010122)98:3<256::aid-ajmg1088>3.0.co;2-d. Am J Med Genet. 2001. PMID: 11169564

2

Clinical and locus heterogeneity in brachydactyly type C.

Robin NH, Gunay-Aygun M, Polinkovsky A, Warman ML, Morrison S. Robin NH, et al. Am J Med Genet. 1997 Jan 31;68(3):369-77. doi: 10.1002/(sici)1096-8628(19970131)68:3<369::aid-ajmg23>3.0.co;2-q. Am J Med Genet. 1997. PMID: 9024575

3

Brachydactyly type C gene maps to human chromsome 12q24.

Polymeropoulos MH, Ide SE, Magyari T, Francomano CA. Polymeropoulos MH, et al. Genomics. 1996 Nov 15;38(1):45-50. doi: 10.1006/geno.1996.0590. Genomics. 1996. PMID: 8954778

4

Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation.

Dobbs MB, Gurnett CA, Robarge J, Gordon JE, Morcuende JA, Bowcock AM. Dobbs MB, et al. J Orthop Res. 2005 Nov;23(6):1490-4. doi: 10.1016/j.orthres.2005.04.011.1100230636. Epub 2005 Jul 11. J Orthop Res. 2005. PMID: 16005596 Free article.

5

Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated families.

Savarirayan R, White SM, Goodman FR, Graham JM Jr, Delatycki MB, Lachman RS, Rimoin DL, Everman DB, Warman ML. Savarirayan R, et al. Am J Med Genet A. 2003 Mar 1;117A(2):136-42. doi: 10.1002/ajmg.a.10924. Am J Med Genet A. 2003. PMID: 12567410

6

A novel locus for brachydactyly type A1 on chromosome 5p13.3-p13.2.

Armour CM, McCready ME, Baig A, Hunter AG, Bulman DE. Armour CM, et al. J Med Genet. 2002 Mar;39(3):186-8. doi: 10.1136/jmg.39.3.186. J Med Genet. 2002. PMID: 11897820 Free PMC article. No abstract available.

7

The mutational spectrum of brachydactyly type C.

Everman DB, Bartels CF, Yang Y, Yanamandra N, Goodman FR, Mendoza-Londono JR, Savarirayan R, White SM, Graham JM Jr, Gale RP, Svarch E, Newman WG, Kleckers AR, Francomano CA, Govindaiah V, Singh L, Morrison S, Thomas JT, Warman ML. Everman DB, et al. Am J Med Genet. 2002 Oct 15;112(3):291-6. doi: 10.1002/ajmg.10777. Am J Med Genet. 2002. PMID: 12357473

8

Mild brachydactyly type A1 maps to chromosome 2q35-q36 and is caused by a novel IHH mutation in a three generation family.

Giordano N, Gennari L, Bruttini M, Mari F, Meloni I, Baldi C, Capoccia S, Geraci S, Merlotti D, Amendola A, Martini G, Nuti R, Gennari C, Renieri A. Giordano N, et al. J Med Genet. 2003 Feb;40(2):132-5. doi: 10.1136/jmg.40.2.132. J Med Genet. 2003. PMID: 12566523 Free PMC article. No abstract available.

9

Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome).

Faiyaz-Ul-Haque M, Ahmad W, Zaidi SH, Haque S, Teebi AS, Ahmad M, Cohn DH, Tsui LC. Faiyaz-Ul-Haque M, et al. Clin Genet. 2002 Jun;61(6):454-8. doi: 10.1034/j.1399-0004.2002.610610.x. Clin Genet. 2002. PMID: 12121354

10

Autosomal dominant hypertension with brachydactyly: an enigmatic form of monogenic hypertension.

Schuster H. Schuster H. Nephrol Dial Transplant. 1998 Jun;13(6):1337-40. doi: 10.1093/ndt/13.6.1337. Nephrol Dial Transplant. 1998. PMID: 9641152 No abstract available.

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