Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Prenatal diagnosis of charcot-marie-tooth disease type 1a by multicolor in situ hybridizationR V Lego L R Martelli; Y Su; L Li; E Lynch; E Mansfield; K H Pua; D F Watson; J Chuech; O HurkoNew York v.47, p.441-50, 1993 American Journal of Medical GeneticsNew York 1993Item não circula. Consulte sua biblioteca.(Acessar) |
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2 |
Material Type: Artigo
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Prenatal diagnosis of charcot-marie-tooth disease type 1a by multicolor in situ hybridizationR V Lego L R Martelli; Y Su; L Li; E Lynch; E Mansfield; K H Pua; D F Watson; J Chuech; O HurkoNew York v.47, p.441-50, 1993 American Journal of Medical GeneticsNew York 1993Item não circula. Consulte sua biblioteca.(Acessar) |
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3 |
Material Type: Artigo
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Mapping of a cerebellar degeneration related protein and DXS304 around the fragile siteHirst, M. C. ; Bell, M. V. ; MacKinnon, R. N. ; Watson, J. E. V. ; Callen, D. ; Sutherland, G. ; Dahl, N. ; Patterson, M. N. ; Schwartz, C. ; Ledbetter, D. ; Ledbetter, S. ; Davies, K. E.American journal of medical genetics, 1991-02, Vol.38 (2-3), p.354-356 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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4 |
Material Type: Artigo
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HLA typing in Bartter syndromeDelaney, Vera ; Watson, A. J. ; Pollack, Marilyn ; Dupont, Bo ; Bourke, E.American journal of medical genetics, 1984-12, Vol.19 (4), p.779-782 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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5 |
Material Type: Artigo
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Mapping of a cerebellar degenertion related protein and DXS304 around the fragile siteHIRST, M. C ; BELL, M. V ; LEDBETTER, S ; DAVIES, K. E ; MACKINNON, R. N ; WATSON, J. E. V ; CALLEN, D ; SUTHERLAND, G ; DAHL, N ; PATTERSON, M. N ; SCHWARTZ, C ; LEDBETTER, DAmerican journal of medical genetics, 1991, Vol.38 (2-3), p.354-356New York, NY: Wiley-LissTexto completo disponível |
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6 |
Material Type: Artigo
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Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease : The NIMH Alzheimer disease genetics initiative: Neuropsychiatric GeneticsCOLLINS, Julianne S ; PERRY, Rodney T ; CAMPBELL, R. Duncan ; GO, Rodney C. P ; WATSON, Bracie JR ; HARRELL, Lindy E ; ACTON, Ronald T ; BLACKER, Deborah ; ALBERT, Marilyn S ; TANZI, Rudolph E ; BASSETT, Susan S ; MCINNIS, Melvin GAmerican journal of medical genetics, 2000, Vol.96 (6), p.823-830New York, NY: Wiley-LissTexto completo disponível |
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7 |
Material Type: Artigo
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Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: The NIMH Alzheimer disease genetics initiativeCollins, Julianne S. ; Perry, Rodney T. ; Watson Jr, Bracie ; Harrell, Lindy E. ; Acton, Ronald T. ; Blacker, Deborah ; Albert, Marilyn S. ; Tanzi, Rudolph E. ; Bassett, Susan S. ; McInnis, Melvin G. ; Campbell, R. Duncan ; Go, Rodney C.P.American journal of medical genetics, 2000-12, Vol.96 (6), p.823-830 [Periódico revisado por pares]New York: John Wiley & Sons, IncTexto completo disponível |
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8 |
Material Type: Artigo
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Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocationWhelan, Alison J. ; Watson, Michael S. ; Porter, Forbes D. ; Steiner, Robert D.American journal of medical genetics, 1995-12, Vol.59 (4), p.492-494 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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9 |
Material Type: Artigo
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Partial monosomy of distal 10q: Three new cases and a reviewWaggoner, Darrel J. ; Chow, Clara K. ; Dowton, S. Bruce ; Watson, Michael S.American journal of medical genetics, 1999-09, Vol.86 (1), p.1-5 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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10 |
Material Type: Artigo
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Deletion of 1q in a patient with acrofacial dysostosisWaggoner, Darrel J. ; Ciske, David J. ; Dowton, S. Bruce ; Watson, Michael S.American journal of medical genetics, 1999-02, Vol.82 (4), p.301-304 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |