Similar articles for PMID: 24639906

Year	Number of Results
1997	2
1998	1
1999	1
2000	4
2001	2
2002	3
2003	4
2004	5
2005	3
2006	4
2007	2
2008	2
2009	6
2010	2
2011	7
2012	6
2013	4
2014	6
2015	2
2016	8
2017	6
2018	9
2019	2
2020	4
2021	7
2022	5
2023	1
2024	0

1

Mandibuloacral Dysplasia Caused by LMNA Mutations and Uniparental Disomy.

Bai S, Lozada A, Jones MC, Dietz HC, Dempsey M, Das S. Bai S, et al. Case Rep Genet. 2014;2014:508231. doi: 10.1155/2014/508231. Epub 2014 Feb 3. Case Rep Genet. 2014. PMID: 24639906 Free PMC article.

2

Mandibuloacral dysplasia type A-associated progeria caused by homozygous LMNA mutation in a family from Southern China.

Luo DQ, Wang XZ, Meng Y, He DY, Chen YM, Ke ZY, Yan M, Huang Y, Chen DF. Luo DQ, et al. BMC Pediatr. 2014 Oct 7;14:256. doi: 10.1186/1471-2431-14-256. BMC Pediatr. 2014. PMID: 25286833 Free PMC article.

3

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C.

Novelli G, Muchir A, Sangiuolo F, Helbling-Leclerc A, D'Apice MR, Massart C, Capon F, Sbraccia P, Federici M, Lauro R, Tudisco C, Pallotta R, Scarano G, Dallapiccola B, Merlini L, Bonne G. Novelli G, et al. Am J Hum Genet. 2002 Aug;71(2):426-31. doi: 10.1086/341908. Epub 2002 Jun 19. Am J Hum Genet. 2002. PMID: 12075506 Free PMC article.

4

Advanced parental age in maternal uniparental disomy (UPD): implications for the mechanism of formation.

Kotzot D. Kotzot D. Eur J Hum Genet. 2004 May;12(5):343-6. doi: 10.1038/sj.ejhg.5201158. Eur J Hum Genet. 2004. PMID: 14747835

5

Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies.

Kortüm F, Chyrek M, Fuchs S, Albrecht B, Gillessen-Kaesbach G, Mütze U, Seemanova E, Tinschert S, Wieczorek D, Rosenberger G, Kutsche K. Kortüm F, et al. Mol Syndromol. 2011 Dec;2(1):27-34. doi: 10.1159/000334317. Epub 2011 Nov 12. Mol Syndromol. 2011. PMID: 22570643 Free PMC article.

6

A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia.

Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK. Garg A, et al. J Clin Endocrinol Metab. 2005 Sep;90(9):5259-64. doi: 10.1210/jc.2004-2560. Epub 2005 Jul 5. J Clin Endocrinol Metab. 2005. PMID: 15998779 Review.

7

The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?

Eggermann T, Oehl-Jaschkowitz B, Dicks S, Thomas W, Kanber D, Albrecht B, Begemann M, Kurth I, Beygo J, Buiting K. Eggermann T, et al. Mol Genet Genomic Med. 2017 Nov;5(6):668-677. doi: 10.1002/mgg3.324. Epub 2017 Sep 22. Mol Genet Genomic Med. 2017. PMID: 29178649 Free PMC article.

8

An inherited LMNA gene mutation in atypical Progeria syndrome.

Doubaj Y, De Sandre-Giovannoli A, Vera EV, Navarro CL, Elalaoui SC, Tajir M, Lévy N, Sefiani A. Doubaj Y, et al. Am J Med Genet A. 2012 Nov;158A(11):2881-7. doi: 10.1002/ajmg.a.35557. Epub 2012 Sep 18. Am J Med Genet A. 2012. PMID: 22991222

9

Fumarase deficiency caused by homozygous P131R mutation and paternal partial isodisomy of chromosome 1.

Zeng WQ, Gao H, Brueton L, Hutchin T, Gray G, Chakrapani A, Olpin S, Shih VE. Zeng WQ, et al. Am J Med Genet A. 2006 May 1;140(9):1004-9. doi: 10.1002/ajmg.a.31186. Am J Med Genet A. 2006. PMID: 16575891

10

Atypical progeroid syndrome due to heterozygous missense LMNA mutations.

Garg A, Subramanyam L, Agarwal AK, Simha V, Levine B, D'Apice MR, Novelli G, Crow Y. Garg A, et al. J Clin Endocrinol Metab. 2009 Dec;94(12):4971-83. doi: 10.1210/jc.2009-0472. Epub 2009 Oct 29. J Clin Endocrinol Metab. 2009. PMID: 19875478 Free PMC article.

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