Bibliographic Details
| Title: |
Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. |
| Authors: |
Celestino-Soper PB; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA., Shaw CA, Sanders SJ, Li J, Murtha MT, Ercan-Sencicek AG, Davis L, Thomson S, Gambin T, Chinault AC, Ou Z, German JR, Milosavljevic A, Sutcliffe JS, Cook EH Jr, Stankiewicz P, State MW, Beaudet AL |
| Source: |
Human molecular genetics [Hum Mol Genet] 2011 Nov 15; Vol. 20 (22), pp. 4360-70. Date of Electronic Publication: 2011 Aug 24. |
| Publication Type: |
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: |
Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: |
MEDLINE Ultimate |
