Thompson EM - Search Results

1

A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.

Feldman GJ, Robin NH, Brueton LA, Robertson E, Thompson EM, Siegel-Bartelt J, Gasser DL, Bailey LC, Zackai EH, Muenke M. Feldman GJ, et al. Among authors: thompson em. Am J Hum Genet. 1995 Apr;56(4):938-43. Am J Hum Genet. 1995. PMID: 7717404 Free PMC article.

2

Apparent cleidocranial dysplasia associated with abnormalities of 8q22 in three individuals.

Brueton LA, Reeve A, Ellis R, Husband P, Thompson EM, Kingston HM. Brueton LA, et al. Among authors: thompson em. Am J Med Genet. 1992 Jun 1;43(3):612-8. doi: 10.1002/ajmg.1320430322. Am J Med Genet. 1992. PMID: 1605259

3

Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda.

Gedeon AK, Colley A, Jamieson R, Thompson EM, Rogers J, Sillence D, Tiller GE, Mulley JC, Gécz J. Gedeon AK, et al. Among authors: thompson em. Nat Genet. 1999 Aug;22(4):400-4. doi: 10.1038/11976. Nat Genet. 1999. PMID: 10431248

4

Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotype.

Brueton LA, Huson SM, Cox PM, Shirley I, Thompson EM, Barnes PR, Price J, Newsom-Davis J, Vincent A. Brueton LA, et al. Among authors: thompson em. Am J Med Genet. 2000 May 1;92(1):1-6. doi: 10.1002/(sici)1096-8628(20000501)92:1<1::aid-ajmg1>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10797415

5

Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation.

Zhao F, Weismann CG, Satoda M, Pierpont ME, Sweeney E, Thompson EM, Gelb BD. Zhao F, et al. Among authors: thompson em. Am J Hum Genet. 2001 Oct;69(4):695-703. doi: 10.1086/323410. Epub 2001 Aug 14. Am J Hum Genet. 2001. PMID: 11505339 Free PMC article.

6

14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements.

Allou L, Lambert L, Amsallem D, Bieth E, Edery P, Destrée A, Rivier F, Amor D, Thompson E, Nicholl J, Harbord M, Nemos C, Saunier A, Moustaïne A, Vigouroux A, Jonveaux P, Philippe C. Allou L, et al. Eur J Hum Genet. 2012 Dec;20(12):1216-23. doi: 10.1038/ejhg.2012.127. Epub 2012 Jun 27. Eur J Hum Genet. 2012. PMID: 22739344 Free PMC article.

7

Is there a monosomy 10qter syndrome?

Mulcahy MT, Pemberton PJ, Thompson E, Watson M. Mulcahy MT, et al. Clin Genet. 1982 Jan;21(1):33-5. doi: 10.1111/j.1399-0004.1982.tb02076.x. Clin Genet. 1982. PMID: 7067162 No abstract available.

8

Necropsy findings in a child with FG syndrome.

Thompson EM, Harding BN, Lake BD, Smith SC. Thompson EM, et al. J Med Genet. 1986 Aug;23(4):372-3. doi: 10.1136/jmg.23.4.372. J Med Genet. 1986. PMID: 3746847 Free PMC article. No abstract available.

9

Extreme genome scrambling in marine planktonic Oikopleura dioica cryptic species.

Plessy C, Mansfield MJ, Bliznina A, Masunaga A, West C, Tan Y, Liu AW, Grašič J, Del Río Pisula MS, Sánchez-Serna G, Fabrega-Torrus M, Ferrández-Roldán A, Roncalli V, Navratilova P, Thompson EM, Onuma T, Nishida H, Cañestro C, Luscombe NM. Plessy C, et al. Among authors: thompson em. Genome Res. 2024 Apr 25;34(3):426-440. doi: 10.1101/gr.278295.123. Genome Res. 2024. PMID: 38621828

10

The influence of anthropogenic regulation and evaporite dissolution on earthquake-triggered ground failure.

Bürgi P, Thompson EM, Allstadt KE, Murray KD, Mason HB, Ahdi SK, Katzenstein D. Bürgi P, et al. Among authors: thompson em. Nat Commun. 2024 Mar 8;15(1):2114. doi: 10.1038/s41467-024-46335-3. Nat Commun. 2024. PMID: 38459018 Free PMC article.

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