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Refinado por: Base de dados/Biblioteca: Springer Nature - Springer Journals All 2022 remover nível superior: Revistas revisadas por pares remover
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11
Integration of Lupinus angustifolius L. (narrow-leafed lupin) genome maps and comparative mapping within legumes
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Integration of Lupinus angustifolius L. (narrow-leafed lupin) genome maps and comparative mapping within legumes

Wyrwa, Katarzyna ; Książkiewicz, Michał ; Szczepaniak, Anna ; Susek, Karolina ; Podkowiński, Jan ; Naganowska, Barbara

Chromosome research, 2016-09, Vol.24 (3), p.355-378 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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12
Human gene polymorphisms and their possible impact on the clinical outcome of SARS-CoV-2 infection
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Human gene polymorphisms and their possible impact on the clinical outcome of SARS-CoV-2 infection

Hashemi, Seyed Mohammad Ali ; Thijssen, Marijn ; Hosseini, Seyed Younes ; Tabarraei, Alijan ; Pourkarim, Mahmoud Reza ; Sarvari, Jamal

Archives of virology, 2021-08, Vol.166 (8), p.2089-2108 [Periódico revisado por pares]

Vienna: Springer Vienna

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13
Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study
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Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study

Karacan, İlker ; Balamir, Ayşe ; Uğurlu, Serdal ; Aydın, Aslı Kireçtepe ; Everest, Elif ; Zor, Seyit ; Önen, Merve Özkılınç ; Daşdemir, Selçuk ; Özkaya, Ozan ; Sözeri, Betül ; Tufan, Abdurrahman ; Yıldırım, Deniz Gezgin ; Yüksel, Selçuk ; Ayaz, Nuray Aktay ; Ömeroğlu, Rukiye Eker ; Öztürk, Kübra ; Çakan, Mustafa ; Söylemezoğlu, Oğuz ; Şahin, Sezgin ; Barut, Kenan ; Adroviç, Amra ; Seyahi, Emire ; Özdoğan, Huri ; Kasapçopur, Özgür ; Turanlı, Eda Tahir

Rheumatology international, 2019-05, Vol.39 (5), p.911-919 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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14
Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease
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Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease

Cangiano, Biagio ; Swee, Du Soon ; Quinton, Richard ; Bonomi, Marco

Human genetics, 2021-01, Vol.140 (1), p.77-111 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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15
Hereditary breast cancer: new genetic developments, new therapeutic avenues
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Hereditary breast cancer: new genetic developments, new therapeutic avenues

Campeau, Philippe M. ; Foulkes, William D. ; Tischkowitz, Marc D.

Human genetics, 2008-08, Vol.124 (1), p.31-42 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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16
large-scale candidate gene association study of age at menarche and age at natural menopause
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large-scale candidate gene association study of age at menarche and age at natural menopause

He, Chunyan ; Kraft, Peter ; Chasman, Daniel I ; Buring, Julie E ; Chen, Constance ; Hankinson, Susan E ; Paré, Guillaume ; Chanock, Stephen ; Ridker, Paul M ; Hunter, David J

Human genetics, 2010-11, Vol.128 (5), p.515-527 [Periódico revisado por pares]

Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag

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17
Marker development, saturation mapping, and high-resolution mapping of the Septoria nodorum blotch susceptibility gene Snn3-B1 in wheat
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Marker development, saturation mapping, and high-resolution mapping of the Septoria nodorum blotch susceptibility gene Snn3-B1 in wheat

Shi, Gongjun ; Zhang, Zengcui ; Friesen, Timothy L. ; Bansal, Urmil ; Cloutier, Sylvie ; Wicker, Thomas ; Rasmussen, Jack B. ; Faris, Justin D.

Molecular genetics and genomics : MGG, 2016-02, Vol.291 (1), p.107-119 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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18
Revisiting Mendelian disorders through exome sequencing
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Revisiting Mendelian disorders through exome sequencing

Ku, Chee-Seng ; Naidoo, Nasheen ; Pawitan, Yudi

Human genetics, 2011-04, Vol.129 (4), p.351-370 [Periódico revisado por pares]

Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag

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19
Humanized mouse models of immunological diseases and precision medicine
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Humanized mouse models of immunological diseases and precision medicine

Shultz, Leonard D. ; Keck, James ; Burzenski, Lisa ; Jangalwe, Sonal ; Vaidya, Shantashri ; Greiner, Dale L. ; Brehm, Michael A.

Mammalian genome, 2019-06, Vol.30 (5-6), p.123-142 [Periódico revisado por pares]

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20
Genetic alterations in uncommon low-grade neuroepithelial tumors: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphology
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Genetic alterations in uncommon low-grade neuroepithelial tumors: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphology

Qaddoumi, Ibrahim ; Orisme, Wilda ; Wen, Ji ; Santiago, Teresa ; Gupta, Kirti ; Dalton, James D. ; Tang, Bo ; Haupfear, Kelly ; Punchihewa, Chandanamali ; Easton, John ; Mulder, Heather ; Boggs, Kristy ; Shao, Ying ; Rusch, Michael ; Becksfort, Jared ; Gupta, Pankaj ; Wang, Shuoguo ; Lee, Ryan P. ; Brat, Daniel ; Peter Collins, V. ; Dahiya, Sonika ; George, David ; Konomos, William ; Kurian, Kathreena M. ; McFadden, Kathryn ; Serafini, Luciano Neder ; Nickols, Hilary ; Perry, Arie ; Shurtleff, Sheila ; Gajjar, Amar ; Boop, Fredrick A. ; Klimo, Paul D. ; Mardis, Elaine R. ; Wilson, Richard K. ; Baker, Suzanne J. ; Zhang, Jinghui ; Wu, Gang ; Downing, James R. ; Tatevossian, Ruth G. ; Ellison, David W.

Acta neuropathologica, 2016-06, Vol.131 (6), p.833-845 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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