The Year in Human and Medical Genetics
Wiley-Blackwell (Verlag)
978-1-57331-851-8 (ISBN)
NOTE: Annals volumes are available for sale as individual books or as a journal. For information on institutional journal subscriptions, please visit http://ordering.onlinelibrary.wiley.com/subs.asp?ref=1749-6632&doi=10.1111/(ISSN)1749-6632.
ACADEMY MEMBERS: Please contact the New York Academy of Sciences directly to place your order (www.nyas.org). Members of the New York Academy of Science receive full-text access to Annals online and discounts on print volumes. Please visit http://www.nyas.org/MemberCenter/Join.aspx for more information about becoming a member.
Jean-Laurent Casanova is the editor of The Year in Human and Medical Genetics: Inborn Errors of Immunity II, Volume 1242, published by Wiley. Mary Ellen Conley is the editor of The Year in Human and Medical Genetics: Inborn Errors of Immunity II, Volume 1242, published by Wiley.
The establishment of early B cell tolerance in humans : lessons from primary immunodeficiency diseases / Eric Meffre Checkpoints of B cell differentiation : visualizing Ig-centric processes / Magdalena A. Berkowska [and others]
DOCK8 deficiency / Helen C. Su, Huie Jing, and Qian Zhang
Molecular mechanisms of the immunological abnormalities in hyper-IgE syndrome / Yoshiyuki Minegishi and Masako Saito
Perspectives on common variable immune deficiency / Joon H. Park, Elena S. Resnick, and Charlotte Cunningham-Rundles
DNA repair : the link between primary immunodeficiency and cancer / Noel FCC de Miranda, Andrea Björkman, and Qiang Pan-Hammarström
Inherited defects causing hemophagocytic lymphohistiocytic syndrome / Geneviève de Saint Basile, Gaël Ménasché, and Sylvain Latour
Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy : known and novel aspects of the syndrome / Kai Kisand and Pärt Peterson
Genetic lessons learned from X-linked Mendelian susceptibility to mycobacterial diseases / Jacinta Bustamante [and others]
IL-10 and IL-10 receptor defects in humans / Erik-Oliver Glocker . [and others]
The case for newborn screening for severe combined immunodeficiency and related disorders / Jennifer M. Puck
Newborn screening for primary immunodeficiencies : beyond SCID and XLA / Stephan Borte [and others]
Homologous recombination-based gene therapy for the primary immunodeficiencies / Matthew Porteus
Erscheint lt. Verlag | 2.3.2012 |
---|---|
Reihe/Serie | Annals of the New York Academy of Sciences |
Verlagsort | Hoboken |
Sprache | englisch |
Maße | 179 x 254 mm |
Gewicht | 324 g |
Themenwelt | Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik |
Naturwissenschaften ► Biologie | |
ISBN-10 | 1-57331-851-5 / 1573318515 |
ISBN-13 | 978-1-57331-851-8 / 9781573318518 |
Zustand | Neuware |
Haben Sie eine Frage zum Produkt? |
aus dem Bereich