Bibliographic Details
| Title: |
The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males. |
| Authors: |
Twigg SR; Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, OX3 9DS, United Kingdom., Matsumoto K, Kidd AM, Goriely A, Taylor IB, Fisher RB, Hoogeboom AJ, Mathijssen IM, Lourenco MT, Morton JE, Sweeney E, Wilson LC, Brunner HG, Mulliken JB, Wall SA, Wilkie AO |
| Source: |
American journal of human genetics [Am J Hum Genet] 2006 Jun; Vol. 78 (6), pp. 999-1010. Date of Electronic Publication: 2006 Apr 28. |
| Publication Type: |
Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: |
Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE |
| Database: |
MEDLINE Ultimate |
