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1
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Artigo
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Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? [Carta]

Amanda G Silva Ana Cristina Victorino Krepischi; Giovana T Torrezan; Leonardo P Capelli; Dirce M Carraro; Carla S D'Angelo; Celia Priszkulnik Koiffmann; Mayana Zatz; Michel Naslavsky; Cibele Masotti; Paulo A Otto; Maria I. W Achatz; Ryan E Mills; Charles Lee; Peter L Pearson; Carla Rosenberg

European Journal of Human Genetics London online, p. 1-3 on-line, 2013

London 2013

Item não circula. Consulte sua biblioteca.(Acessar)

2
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants
Material Type:
Artigo
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Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

Souzeau, Emmanuelle ; Siggs, Owen M ; Zhou, Tiger ; Galanopoulos, Anna ; Hodson, Trevor ; Taranath, Deepa ; Mills, Richard A ; Landers, John ; Pater, John ; Smith, James E ; Elder, James E ; Rait, Julian L ; Giles, Paul ; Phakey, Vivek ; Staffieri, Sandra E ; Kearns, Lisa S ; Dubowsky, Andrew ; Mackey, David A ; Hewitt, Alex W ; Ruddle, Jonathan B ; Burdon, Kathryn P ; Craig, Jamie E

European journal of human genetics : EJHG, 2017-06, Vol.25 (7), p.839-847 [Periódico revisado por pares]

England: Nature Publishing Group

Texto completo disponível

3
The effect of sample size on polygenic hazard models for prostate cancer
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Artigo
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The effect of sample size on polygenic hazard models for prostate cancer

Karunamuni, Roshan A ; Huynh-Le, Minh-Phuong ; Fan, Chun C ; Eeles, Rosalind A ; Easton, Douglas F ; Kote-Jarai, ZSofia ; Amin Al Olama, Ali ; Benlloch Garcia, Sara ; Muir, Kenneth ; Gronberg, Henrik ; Wiklund, Fredrik ; Aly, Markus ; Schleutker, Johanna ; Sipeky, Csilla ; Tammela, Teuvo L J ; Nordestgaard, Børge G ; Key, Tim J ; Travis, Ruth C ; Neal, David E ; Donovan, Jenny L ; Hamdy, Freddie C ; Pharoah, Paul ; Pashayan, Nora ; Khaw, Kay-Tee ; Thibodeau, Stephen N ; McDonnell, Shannon K ; Schaid, Daniel J ; Maier, Christiane ; Vogel, Walther ; Luedeke, Manuel ; Herkommer, Kathleen ; Kibel, Adam S ; Cybulski, Cezary ; Wokolorczyk, Dominika ; Kluzniak, Wojciech ; Cannon-Albright, Lisa ; Brenner, Hermann ; Schöttker, Ben ; Holleczek, Bernd ; Park, Jong Y ; Sellers, Thomas A ; Lin, Hui-Yi ; Slavov, Chavdar ; Kaneva, Radka ; Mitev, Vanio ; Batra, Jyotsna ; Clements, Judith A ; Spurdle, Amanda ; Teixeira, Manuel R ; Paulo, Paula ; Maia, Sofia ; Pandha, Hardev ; Michael, Agnieszka ; Mills, Ian G ; Andreassen, Ole A ; Dale, Anders M ; Seibert, Tyler M

European journal of human genetics : EJHG, 2020-10, Vol.28 (10), p.1467-1475 [Periódico revisado por pares]

England: Nature Publishing Group

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4
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia
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Artigo
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Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia

Matsumoto, N ; Leventer, R J ; Kuc, J A ; Mewborn, S K ; Dudlicek, L L ; Ramocki, M B ; Pilz, D T ; Mills, P L ; Das, S ; Ross, M E ; Ledbetter, D H ; Dobyns, W B

European journal of human genetics : EJHG, 2001-01, Vol.9 (1), p.5-12 [Periódico revisado por pares]

England: Nature Publishing Group

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5
Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population
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Artigo
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Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population

PARLE-MCDERMOTT, Anne ; KIRKE, Peadar N ; SCOTT, John M ; MILLS, James L ; MOLLOY, Anne M ; COX, Christopher ; O'LEARY, Valerie B ; PANGILINAN, Faith ; CONLEY, Mary ; CLEARY, Laura ; BRODY, Lawrence C

European journal of human genetics : EJHG, 2006-06, Vol.14 (6), p.768-772 [Periódico revisado por pares]

Avenel, NJ: Nature Publishing

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6
Does germ-line deletion of the PIP gene constitute a widespread risk for cancer?
Material Type:
Artigo
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Does germ-line deletion of the PIP gene constitute a widespread risk for cancer?

Silva, Amanda G ; Krepischi, Ana C V ; Torrezan, Giovana T ; Capelli, Leonardo P ; Carraro, Dirce M ; D'Angelo, Carla S ; Koiffmann, Celia P ; Zatz, Mayana ; Naslavsky, Michel S ; Masotti, Cibele ; Otto, Paulo A ; Achatz, Maria I W ; Mills, Ryan E ; Lee, Charles ; Pearson, Peter L ; Rosenberg, Carla

European journal of human genetics : EJHG, 2014-03, Vol.22 (3), p.307-309 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Erratum: Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants
Material Type:
Artigo
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Erratum: Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

Souzeau, Emmanuelle ; Siggs, Owen M ; Zhou, Tiger ; Galanopoulos, Anna ; Hodson, Trevor ; Taranath, Deepa ; Mills, Richard A ; Landers, John ; Pater, John ; Smith, James E ; Elder, James E ; Rait, Julian L ; Giles, Paul ; Phakey, Vivek ; Staffieri, Sandra E ; Kearns, Lisa S ; Dubowsky, Andrew ; Mackey, David A ; Hewitt, Alex W ; Ruddle, Jonathan B ; Burdon, Kathryn P ; Craig, Jamie E

European journal of human genetics : EJHG, 2017-10, Vol.25 (11), p.1290-1290 [Periódico revisado por pares]

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8
Ovarian Cancer: Identification of remodeling and spacing factor 1 (rsf-1, HBXAP) at chromosome 11q13 as a putative oncogene in ovarian cancer
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Artigo
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Ovarian Cancer: Identification of remodeling and spacing factor 1 (rsf-1, HBXAP) at chromosome 11q13 as a putative oncogene in ovarian cancer

Hennessy, Bryan T ; Nanjundan, Meera ; Cheng, Kwai Wa ; Nolden, Laura ; Mills, Gordon B

European journal of human genetics : EJHG, 2006-04, Vol.14 (4), p.381-383 [Periódico revisado por pares]

Leiden: Nature Publishing Group

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Deste Autor:

  1. Carraro, D
  2. Torrezan, G
  3. Lee, C
  4. Silva, A
  5. Achatz, M

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