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TitleDateReferenceAuthorsCall #ISSN
An exonic mutation in the "HuP2" paired domain gene causes Waardenburg's syndrome [Brazilian data; with comments by MA Walter and PN Goodfellow, see below] 1992 Nature 355 (): 637-41
  • C T Baldwin
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium 1992 American Journal of human genetics 50 (5): 902-13
  • L A Farrer
Waardenburg's syndrome patients have mutations in the human homologue of the "Pax-3" paired box gene [with comments by MA Walter and PN Goodfellow, see below] 1992 Nature 355 (): 635-6
  • M Tassabehji
Disease and development [comments on M Tassabehji and others, and CT Baldwin and others, see above] 1992 Nature 355 (): 590-1
  • M A Walter
  • P N Goodfellow
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