Larsson C - Search Results

1

Two Chinese families with pulverulent congenital cataracts and deltaG91 CRYBA1 mutations.

Lu S, Zhao C, Jiao H, Kere J, Tang X, Zhao F, Zhang X, Zhao K, Larsson C. Lu S, et al. Among authors: larsson c. Mol Vis. 2007 Jul 13;13:1154-60. Mol Vis. 2007. PMID: 17653060

2

Genetic mapping of the multiple endocrine neoplasia type 1 locus at 11q13.

Teh BT, Cardinal J, Shepherd J, Hayward NK, Weber G, Cameron D, Larsson C. Teh BT, et al. Among authors: larsson c. J Intern Med. 1995 Sep;238(3):249-53. doi: 10.1111/j.1365-2796.1995.tb00931.x. J Intern Med. 1995. PMID: 7673855

3

Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.

Wong FK, Hagberg C, Karsten A, Larson O, Gustavsson M, Huggare J, Larsson C, Teh BT, Linder-Aronson S. Wong FK, et al. Among authors: larsson c. Cleft Palate Craniofac J. 2000 Jul;37(4):357-62. doi: 10.1597/1545-1569_2000_037_0357_laocri_2.3.co_2. Cleft Palate Craniofac J. 2000. PMID: 10912714

4

Dominantly inherited familial myasthenia gravis as a separate genetic entity without involvement of defined candidate gene loci.

Li F, Szobor A, Croxen R, Anselmo V, Yuan QP, Lindblad K, Schalling M, Komoly S, Beeson D, Larsson C. Li F, et al. Among authors: larsson c. Int J Mol Med. 2001 Mar;7(3):289-94. doi: 10.3892/ijmm.7.3.289. Int J Mol Med. 2001. PMID: 11179509

5

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome.

Wong FK, Koillinen H, Rautio J, Teh BT, Ranta R, Karsten A, Larson O, Linder-Aronson S, Huggare J, Larsson C, Kere J. Wong FK, et al. Among authors: larsson c. J Med Genet. 2001 Mar;38(3):198-202. doi: 10.1136/jmg.38.3.198. J Med Genet. 2001. PMID: 11303516 Free PMC article. No abstract available.

6

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.

Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J. Koillinen H, et al. Among authors: larsson c. Eur J Hum Genet. 2001 Oct;9(10):747-52. doi: 10.1038/sj.ejhg.5200713. Eur J Hum Genet. 2001. PMID: 11781685

7

Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.

Peyrard-Janvid M, Pegelow M, Koillinen H, Larsson C, Fransson I, Rautio J, Hukki J, Larson O, Karsten AL, Kere J. Peyrard-Janvid M, et al. Among authors: larsson c. Eur J Hum Genet. 2005 Dec;13(12):1261-7. doi: 10.1038/sj.ejhg.5201493. Eur J Hum Genet. 2005. PMID: 16160700

8

A novel locus (RP33) for autosomal dominant retinitis pigmentosa mapping to chromosomal region 2cen-q12.1.

Zhao C, Lu S, Zhou X, Zhang X, Zhao K, Larsson C. Zhao C, et al. Among authors: larsson c. Hum Genet. 2006 Jul;119(6):617-23. doi: 10.1007/s00439-006-0168-3. Epub 2006 Apr 13. Hum Genet. 2006. PMID: 16612614

9

Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes.

Pegelow M, Peyrard-Janvid M, Zucchelli M, Fransson I, Larson O, Kere J, Larsson C, Karsten A. Pegelow M, et al. Among authors: larsson c. Eur J Orthod. 2008 Apr;30(2):169-75. doi: 10.1093/ejo/cjm097. Epub 2008 Jan 21. Eur J Orthod. 2008. PMID: 18209213

10

Novel and recurrent KIF21A mutations in congenital fibrosis of the extraocular muscles type 1 and 3.

Lu S, Zhao C, Zhao K, Li N, Larsson C. Lu S, et al. Among authors: larsson c. Arch Ophthalmol. 2008 Mar;126(3):388-94. doi: 10.1001/archopht.126.3.388. Arch Ophthalmol. 2008. PMID: 18332320

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