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1
3D Reconstruction of the Mouse's Mesonephros
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Artigo
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3D Reconstruction of the Mouse's Mesonephros

Vazquez, M.-D. ; Bouchet, P. ; Mallet, J.-L. ; Foliguet, B. ; Gérard, H. ; LeHeup, B.

Anatomia, histologia, embryologia, 1998-10, Vol.27 (5), p.283-287 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
46, X, i(Xq) karyotype in a patient with hypoplastic left heart
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Artigo
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46, X, i(Xq) karyotype in a patient with hypoplastic left heart

Shah, Ashok ; Fay, John E. ; Ford, Sally ; Holden, Jeanette J. A.

Clinical genetics, 1985-08, Vol.28 (2), p.178-179 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

Sem texto completo

3
46,XY/48,XXY,+8 in a male with clinical and dermatoglyphic features of mosaic trisomy 8 syndrome
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Artigo
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46,XY/48,XXY,+8 in a male with clinical and dermatoglyphic features of mosaic trisomy 8 syndrome

Casey, Pamela A. ; Clark, Constance E. ; Cowell, Henry R.

Clinical genetics, 1981-07, Vol.20 (1), p.60-63 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

Sem texto completo

4
48, XXXY Klinefelter syndrome and nail-patella syndrome in the same child
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Artigo
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48, XXXY Klinefelter syndrome and nail-patella syndrome in the same child

Jansen, Jette ; Hansen, Erik ; Hobolth, Niels ; Jacobsen, Petrea ; Mikkelsen, Margareta

Clinical genetics, 1976-02, Vol.9 (2), p.163-168 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

Sem texto completo

5
48, XYY,+13 Karyotype in a liveborn infant
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Artigo
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48, XYY,+13 Karyotype in a liveborn infant

Crolla, John A. ; Machin, Geoffrey A.

Clinical genetics, 1980-01, Vol.17 (1), p.31-34 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

Sem texto completo

6
48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome
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Artigo
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48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome

Tartaglia, Nicole ; Ayari, Natalie ; Howell, Susan ; D'Epagnier, Cheryl ; Zeitler, Philip

Acta Paediatrica, 2011-06, Vol.100 (6), p.851-860 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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7
Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes
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Artigo
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Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes

Taibjee, S.M. ; Bennett, D.C. ; Moss, C.

British journal of dermatology (1951), 2004-08, Vol.151 (2), p.269-282 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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8
Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia
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Artigo
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Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia

Li, Xiaxin ; Leteurtre, François ; Rocha, Vanderson ; Guardiola, Philippe ; Berger, Roland ; Daniel, Marie‐Therese ; Noguera, Maria Helena ; Maarek, Odile ; Roux, Gwenaëlle L. E. ; De La Salmonière, Pauline ; Richard, Patrice ; Gluckman, Eliane

British journal of haematology, 2003-03, Vol.120 (5), p.836-845 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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9
Acetaldehyde production by major oral microbes
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Artigo
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Acetaldehyde production by major oral microbes

Moritani, K ; Takeshita, T ; Shibata, Y ; Ninomiya, T ; Kiyohara, Y ; Yamashita, Y

Oral diseases, 2015-09, Vol.21 (6), p.748-754 [Periódico revisado por pares]

Denmark: Blackwell Publishing Ltd

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10
Adenovirus necrotizing hepatitis complicating atypical teratoid rhabdoid tumor
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Artigo
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Adenovirus necrotizing hepatitis complicating atypical teratoid rhabdoid tumor

McKillop, Sarah J. ; Belletrutti, Mark J. ; Lee, Bonita E. ; Yap, Jason Y. ; Noga, Michelle L. ; Desai, Sunil J. ; Sergi, Consolato

Pediatrics international, 2015-10, Vol.57 (5), p.974-977 [Periódico revisado por pares]

Australia: Blackwell Publishing Ltd

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