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Results: 1-3 |
Results: 3
High Incidence of Later-Onset Fabry Disease Revealed by Newborn Screening
Authors: Spada, Marco Pagliardini, Severo Yasuda, Makiko Tukel, Turgut Thiagarajan, Geetha Sakuraba, Hitoshi Ponzone, Alberto Desnick, Robert J
Citation: Spada, Marco et al., High Incidence of Later-Onset Fabry Disease Revealed by Newborn Screening, American journal of human genetics , 79(1), 2006, pp. 31-40
Homozygous Nonsense Mutations in TWIST2 Cause Setleis Syndrome
Authors: Tukel, Turgut .o.i., Dra.en Al-Gazali, Lihadh I. Erazo, Mónica Desnick, Robert J.
Citation: Tukel, Turgut et al., Homozygous Nonsense Mutations in TWIST2 Cause Setleis Syndrome, American journal of human genetics (Online) AJHG , 87(2), 2010, pp. 289-296
Crohn Disease: Frequency and Nature of CARD15 Mutations in Ashkenazi and Sephardi/Oriental Jewish Families
Authors: Tukel, Turgut Present, Daniel Rachmilewitz, Daniel Mayer, Lloyd Grant, Deniera Risch, Neil Shalata, Adel Desnick, Robert J.
Citation: Tukel, Turgut et al., Crohn Disease: Frequency and Nature of CARD15 Mutations in Ashkenazi and Sephardi/Oriental Jewish Families, American journal of human genetics , 74(4), 2004, pp. 623-636
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