Propensity for paternal inheritance of de novo mutations in Alexander disease-Reference-Cited by-同舟云学术

Propensity for paternal inheritance of de novo mutations in Alexander disease

Published:2005-12-20 Issue:1-2 Volume:119 Page:137-144
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Li Rong,Johnson Anne B.,Salomons Gajja S.,van der Knaap Marjo S.,Rodriguez Diana,Boespflug-Tanguy Odile,Gorospe J. Rafael,Goldman James E.,Messing Albee,Brenner Michael

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-005-0116-7.pdf

Reference35 articles.

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2. Cronn R, Cedroni M, Haselkorn T, Grover C, Wendel JF (2002) PCR-mediated recombination in amplification products derived from polyploid cotton. Theor Appl Genet 104:482–489

3. Crow JF (2000) The origins, patterns and implications of human spontaneous mutation. Nat Rev Genet 1:40–47

4. den Dunnen JT, Antonarakis SE (2001) Nomenclature for the description of human sequence variations. Hum Genet 109:121–124

5. Glaser RL, Jiang W, Boyadjiev SA, Tran AK, Zachary AA, Van Maldergem L, Johnson D, Walsh S, Oldridge M, Wall SA, Wilkie AO, Jabs EW (2000) Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome. Am J Hum Genet 66:768–777

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