Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Livro
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Goethe Yearbook 31Sarah Vandegrift. Eldridge Fred Amrine; Frederick Amrine; Claire Baldwin; Walt Maierhofer; Waltraud Maierhofer Me Me; Malte Meyer; Malte Hendrik Meyer; Carl Niekerk; Saurabh Pal Power Power Powers; Daniel Purdy; Michael Saman; Patricia Anne Simpson; Margaret Strair; Michael Swellander; Brian Tucker; David E Wellbery; Matthew Childs; Sally Hatch Gray; Joseph A Haydt; Eleanor ter Horst; Steven R Huff; Peter Höyng; Joseph D O'NeilRochester Boydell & Brewer, Incorporated 2024Acesso online |
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2 |
Material Type: Artigo
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How ancestry influences the chances of finding unrelated donors an investigation in admixed bBraziliansKelly Nunes Vitor R. C Aguiar; Márcio Silva; Alexandre C Sena; Danielli C. M. de Oliveira; Carla L Dinardo; Fernanda S. G Kehdy; Eduardo Tarazona-Santos; Vanderson G Rocha; Anna Barbara F Carneiro-Proietti; Paula Loureiro; Miriam V Flor-Park; Claudia Maximo; Shannon Kelly; Brian Custer; Bruce S Weir; Ester C Sabino; Luís Cristóvão Porto; Diogo MeyerFrontiers in Immunology Lausanne v. 11, art. 584950, 2020Lausanne 2020Acesso online. A biblioteca também possui exemplares impressos. |
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3 |
Material Type: Livro
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The new economic sociology a readerFrank DobbinPrinceton, N.J. Princeton University Press c2004Localização: EACH - Esc. Artes, Ciências e Humanidades (306.3 N532 e.2 ) e outros locais(Acessar) |
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4 |
Material Type: Livro
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Urban ecology an international perspective on the interaction between humans and natureJohn M MarzluffNew York Springer c2008Localização: EACH - Esc. Artes, Ciências e Humanidades (304.2 U72 ) e outros locais(Acessar) |
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5 |
Material Type: E-Book
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Diseases of the kidney & urinary tractRobert W Schrier; R2 Library (Online service)Philadelphia : Wolters Kluwer Health/Lippincott Williams & Wilkins c2007Acesso online. A biblioteca também possui exemplares impressos. |
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6 |
Material Type: Artigo
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Identification of pharmacogenetic variants from large scale next generation sequencing data in the Saudi populationGoljan, Ewa ; Abouelhoda, Mohammed ; ElKalioby, Mohamed M ; Jabaan, Amjad ; Alghithi, Nada ; Meyer, Brian F ; Monies, Dorota Patel, Girijesh KumarPloS one, 2022-01, Vol.17 (1), p.e0263137-e0263137 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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7 |
Material Type: Artigo
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Biallelic UFM1 and UFC1 mutations expand the essential role of ufmylation in brain developmentNahorski, Michael S ; Maddirevula, Sateesh ; Ishimura, Ryosuke ; Alsahli, Saud ; Brady, Angela F ; Begemann, Anaïs ; Mizushima, Tsunehiro ; Guzmán-Vega, Francisco J ; Obata, Miki ; Ichimura, Yoshinobu ; Alsaif, Hessa S ; Anazi, Shams ; Ibrahim, Niema ; Abdulwahab, Firdous ; Hashem, Mais ; Monies, Dorota ; Abouelhoda, Mohamed ; Meyer, Brian F ; Alfadhel, Majid ; Eyaid, Wafa ; Zweier, Markus ; Steindl, Katharina ; Rauch, Anita ; Arold, Stefan T ; Woods, C Geoffrey ; Komatsu, Masaaki ; Alkuraya, Fowzan SBrain (London, England : 1878), 2018-07, Vol.141 (7), p.1934-1945 [Periódico revisado por pares]England: Oxford University PressTexto completo disponível |
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8 |
Material Type: Artigo
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Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid DyshormonogenesisZou, Minjing ; Alzahrani, Ali S ; Al-Odaib, Ali ; Alqahtani, Mohammad A ; Babiker, Omer ; Al-Rijjal, Roua A ; BinEssa, Huda A ; Kattan, Walaa E ; Al-Enezi, Anwar F ; Al Qarni, Ali ; Al-Faham, Manar S A ; Baitei, Essa Y ; Alsagheir, Afaf ; Meyer, Brian F ; Shi, YufeiThe journal of clinical endocrinology and metabolism, 2018-05, Vol.103 (5), p.1889-1898 [Periódico revisado por pares]Washington, DC: Endocrine SocietyTexto completo disponível |
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9 |
Material Type: Artigo
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Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic ricketsBinEssa, Huda A. ; Zou, Minjing ; Al-Enezi, Anwar F. ; Alomrani, Basma ; Al-Faham, Manar S.A. ; Al-Rijjal, Roua A. ; Meyer, Brian F. ; Shi, YufeiBone (New York, N.Y.), 2019-08, Vol.125, p.186-193 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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10 |
Material Type: Artigo
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Homozygous Mutations in ADAMTS10 and ADAMTS17 Cause Lenticular Myopia, Ectopia Lentis, Glaucoma, Spherophakia, and Short StatureMorales, Jose ; Al-Sharif, Latifa ; Khalil, Dania S. ; Shinwari, Jameela M.A. ; Bavi, Prashant ; Al-Mahrouqi, Rahima A. ; Al-Rajhi, Ali ; Alkuraya, Fowzan S. ; Meyer, Brian F. ; Al Tassan, NadaAmerican journal of human genetics, 2009-11, Vol.85 (5), p.558-568 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |