Somer M - Search Results

1

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

2

[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.

3

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

4

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.

5

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

6

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.

7

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

8

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

9

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.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

86 results

Search Page