Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
2 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.
JAMA Pediatr. 2017 Dec 4;171(12):e173438. doi: 10.1001/jamapediatrics.2017.3438. Epub 2017 Dec 4.
JAMA Pediatr. 2017.
PMID: 28973083
Free PMC article.
Pontine tegmental cap dysplasia with a 2q13 microdeletion involving the NPHP1 gene: insights into malformations of the mid-hindbrain.
Macferran KM, Buchmann RF, Ramakrishnaiah R, Griebel ML, Sanger WG, Saronwala A, Schaefer GB.
Macferran KM, et al. Among authors: saronwala a.
Semin Pediatr Neurol. 2010 Mar;17(1):69-74. doi: 10.1016/j.spen.2010.02.014.
Semin Pediatr Neurol. 2010.
PMID: 20434703
Item in Clipboard
Cite
Cite