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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Anne M. Slavotinek

Department of Pediatrics

U.C.S.F.

Room U585P

531 Parnassus Street

USA

[email]@nhgri.nih.gov

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Pediatrics, U.C.S.F., Room U585P, 531 Parnassus Street, USA. 2003
  • National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland 20892, USA. 2000 - 2002
  • University Department of Medical Genetics, St Mary's Hospital, Manchester, UK. 1999

References

  1. Non-syndromic hemihyperplasia in a male and his mother. Slavotinek, A.M., Collins, M.T., Muenke, M. Am. J. Med. Genet. A (2003) [Pubmed]
  2. Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients. Slavotinek, A.M., Searby, C., Al-Gazali, L., Hennekam, R.C., Schrander-Stumpel, C., Orcana-Losa, M., Pardo-Reoyo, S., Cantani, A., Kumar, D., Capellini, Q., Neri, G., Zackai, E., Biesecker, L.G. Hum. Genet. (2002) [Pubmed]
  3. Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal defect, and marfanoid features: possible PHACE syndrome. Slavotinek, A.M., Dubovsky, E., Dietz, H.C., Lacbawan, F. Am. J. Med. Genet. (2002) [Pubmed]
  4. Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes. Slavotinek, A.M., Tifft, C.J. J. Med. Genet. (2002) [Pubmed]
  5. Unfolding the role of chaperones and chaperonins in human disease. Slavotinek, A.M., Biesecker, L.G. Trends Genet. (2001) [Pubmed]
  6. Phenotypic overlap of McKusick-Kaufman syndrome with bardet-biedl syndrome: a literature review. Slavotinek, A.M., Biesecker, L.G. Am. J. Med. Genet. (2000) [Pubmed]
  7. Brachydactyly type B: case report and further evidence for clinical heterogeneity. Slavotinek, A., Clayton-Smith, J. Clin. Dysmorphol. (1999) [Pubmed]
 
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