American Journal of Human Genetics 1998 Andre Reis - Abstracts
| American Journal of Human Genetics 1998 Andre Reis | |||||
| Title | Subject | Authors | |||
|---|---|---|---|---|---|
| Gene localization for an autosomal dominant familial periodic fever to 12p13. | Biological sciences | John Mulley, Meredith Wilson, Andre Reis, Kathrin Saar, Gerry Hewitt, Franz Rushendorf, Hilary Phillips, Alison Colley, David Sillence | |||
| Genotype/phenotype correlation in autosomal recessive lamellar ichthyosis. | Biological sciences | Hans Christian Hennies, Andre Reis, Wolfgang Kuster, Victor Wiebe, Alice Krebsova | |||
| Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis. | Biological sciences | Ans M.W. van den Ouweland, Robert D. Nicholls, Marc Lalande, Bernhard Horsthemke, Pascale Hilbert, Sue Malcolm, Markus M. Nothen, Peter Meinecke, Gabriele Gillessen-Kaesbach, Andre Reis, Gert Matthijs, Dicky J.J. Halley, Karin Buiting, Barbel Dittrich, Stephanie Gross, Christina Lich, Claudia Farber, Tina Buchholz, Ellie Smith, Joachim Burger, Ulli Barth-Witte, Bart Janssen, Dvorah Abeliovich, Israela Lerer, Connie Schrander-Stumpel, Hubert Smeets, Anne Gardner, Kathie Friend, Astrid Schulze, Hannaleena Kokkonen, Lionel Van Maldergem, Guillermo Glover, Pablo Carbonell, Patrick Willems | |||
| The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.(Statistical Data Included) | Biological sciences | Franz Ruschendorf, Andre Reis, Friedhelm Hildebrandt, Martin Vollmer, Martin Jung, Rainer Ruf, Thomas Wienker, Reto Krapf | |||
This website is not affiliated with document authors or copyright owners. This page is provided for informational purposes only. Unintentional errors are possible.