Somer M - Search Results

1

[CATCH-22: a microdeletion of chromosome 22 behind the polymorphous syndrome].

Somer M, Ignatius J, Vehmanen P, Keinänen M, Haapanen ML. Somer M, et al. Duodecim. 1997;113(12):1115-22. Duodecim. 1997. PMID: 11466836 Review. Finnish. No abstract available.

2

Velocardiofacial syndrome: analysis of phoniatric and other clinical findings.

Haapanen ML, Somer M. Haapanen ML, et al. Among authors: somer m. Folia Phoniatr (Basel). 1993;45(5):239-46. doi: 10.1159/000266268. Folia Phoniatr (Basel). 1993. PMID: 8253447

3

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region.

Wright TJ, Ricke DO, Denison K, Abmayr S, Cotter PD, Hirschhorn K, Keinänen M, McDonald-McGinn D, Somer M, Spinner N, Yang-Feng T, Zackai E, Altherr MR. Wright TJ, et al. Among authors: somer m. Hum Mol Genet. 1997 Feb;6(2):317-24. doi: 10.1093/hmg/6.2.317. Hum Mol Genet. 1997. PMID: 9063753

4

18q-syndrome: brain MRI shows poor differentiation of gray and white matter on T2-weighted images.

Linnankivi TT, Autti TH, Pihko SH, Somer MS, Tienari PJ, Wirtavuori KO, Valanne LK. Linnankivi TT, et al. J Magn Reson Imaging. 2003 Oct;18(4):414-9. doi: 10.1002/jmri.10383. J Magn Reson Imaging. 2003. PMID: 14508777

5

Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23); report of familial cryptic chromosome t(18q; 10p) translocations.

Dostal A, Linnankivi T, Somer M, Kähkönen M, Litzman J, Tienari P. Dostal A, et al. Among authors: somer m. Int J Immunogenet. 2007 Jun;34(3):143-7. doi: 10.1111/j.1744-313X.2007.00652.x. Int J Immunogenet. 2007. PMID: 17504501

6

Shprintzen-Goldberg syndrome: fourteen new patients and a clinical analysis.

Robinson PN, Neumann LM, Demuth S, Enders H, Jung U, König R, Mitulla B, Müller D, Muschke P, Pfeiffer L, Prager B, Somer M, Tinschert S. Robinson PN, et al. Among authors: somer m. Am J Med Genet A. 2005 Jun 15;135(3):251-62. doi: 10.1002/ajmg.a.30431. Am J Med Genet A. 2005. PMID: 15884042

7

Distal trisomy 14q syndrome; a case report.

Markkanen A, Somer M, Nordström AM. Markkanen A, et al. Among authors: somer m. Clin Genet. 1984 Sep;26(3):231-4. doi: 10.1111/j.1399-0004.1984.tb04373.x. Clin Genet. 1984. PMID: 6478645 No abstract available.

8

New syndrome: a digito-reno-cerebral syndrome.

Eronen M, Somer M, Gustafsson B, Holmberg C. Eronen M, et al. Among authors: somer m. Am J Med Genet. 1985 Oct;22(2):281-5. doi: 10.1002/ajmg.1320220209. Am J Med Genet. 1985. PMID: 4050858 No abstract available.

9

Cerebellar hypoplasia and Cohen syndrome: a confirmed association.

Waite A, Somer M, O'Driscoll M, Millen K, Manson FD, Chandler KE. Waite A, et al. Among authors: somer m. Am J Med Genet A. 2010 Sep;152A(9):2390-3. doi: 10.1002/ajmg.a.33569. Am J Med Genet A. 2010. PMID: 20683995 No abstract available.

10

Familial Sotos syndrome is caused by a novel 1 bp deletion of the NSD1 gene.

Höglund P, Kurotaki N, Kytölä S, Miyake N, Somer M, Matsumoto N. Höglund P, et al. Among authors: somer m. J Med Genet. 2003 Jan;40(1):51-4. doi: 10.1136/jmg.40.1.51. J Med Genet. 2003. PMID: 12525543 Free PMC article. No abstract available.

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