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Refinado por: Nome da Publicação: American Journal Of Medical Genetics remover
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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 hybridization

R V Lego L R Martelli; Y Su; L Li; E Lynch; E Mansfield; K H Pua; D F Watson; J Chuech; O Hurko

New York v.47, p.441-50, 1993 American Journal of Medical Genetics

New York 1993

Item não circula. Consulte sua biblioteca.(Acessar)

2
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Artigo
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Prenatal diagnosis of charcot-marie-tooth disease type 1a by multicolor in situ hybridization

R V Lego L R Martelli; Y Su; L Li; E Lynch; E Mansfield; K H Pua; D F Watson; J Chuech; O Hurko

New York v.47, p.441-50, 1993 American Journal of Medical Genetics

New York 1993

Item não circula. Consulte sua biblioteca.(Acessar)

3
Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site
Material Type:
Artigo
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Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site

Hirst, 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 Company

Texto completo disponível

4
HLA typing in Bartter syndrome
Material Type:
Artigo
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HLA typing in Bartter syndrome

Delaney, 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 Company

Texto completo disponível

5
Mapping of a cerebellar degenertion related protein and DXS304 around the fragile site
Material Type:
Artigo
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Mapping of a cerebellar degenertion related protein and DXS304 around the fragile site

HIRST, 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, D

American journal of medical genetics, 1991, Vol.38 (2-3), p.354-356

New York, NY: Wiley-Liss

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6
Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease : The NIMH Alzheimer disease genetics initiative: Neuropsychiatric Genetics
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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 Genetics

COLLINS, 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 G

American journal of medical genetics, 2000, Vol.96 (6), p.823-830

New York, NY: Wiley-Liss

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7
Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: The NIMH Alzheimer disease genetics initiative
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

Collins, 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, Inc

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8
Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocation
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Artigo
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Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocation

Whelan, 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 Company

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9
Partial monosomy of distal 10q: Three new cases and a review
Material Type:
Artigo
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Partial monosomy of distal 10q: Three new cases and a review

Waggoner, 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 Company

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10
Deletion of 1q in a patient with acrofacial dysostosis
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Artigo
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Deletion of 1q in a patient with acrofacial dysostosis

Waggoner, 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 Company

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Deste Autor:

  1. Watson, D
  2. Hurko, O
  3. Lego, R
  4. Mansfield, E
  5. Lynch, E

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