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
4 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Severe epileptic encephalopathy associated with compound heterozygosity of THG1L variants in the Ashkenazi Jewish population.
Am J Med Genet A. 2021 May;185(5):1589-1597. doi: 10.1002/ajmg.a.62147. Epub 2021 Mar 8.
Am J Med Genet A. 2021.
PMID: 33682303
Recommendation of premarital genetic screening in the Syrian Jewish community based on mutation carrier frequencies within Syrian Jewish cohorts.
Zeevi DA, Chung WK, Levi C, Scher SY, Bringer R, Kahan Y, Muallem H, Benel R, Hirsch Y, Weiden T, Ekstein A, Ekstein J.
Zeevi DA, et al. Among authors: ekstein a.
Mol Genet Genomic Med. 2021 Aug;9(8):e1756. doi: 10.1002/mgg3.1756. Epub 2021 Jul 20.
Mol Genet Genomic Med. 2021.
PMID: 34288589
Free PMC article.
Item in Clipboard
Carrier frequency of two BBS2 mutations in the Ashkenazi population.
Fedick A, Jalas C, Abeliovich D, Krakinovsky Y, Ekstein J, Ekstein A, Treff NR.
Fedick A, et al. Among authors: ekstein a.
Clin Genet. 2014 Jun;85(6):578-82. doi: 10.1111/cge.12231. Epub 2013 Jul 28.
Clin Genet. 2014.
PMID: 23829372
Item in Clipboard
Screening for neonatal hypothyroidism in Israel.
Sack J, Amado O, Frucht H, Ekstein A.
Sack J, et al. Among authors: ekstein a.
Isr J Med Sci. 1981 Apr;17(4):294-5.
Isr J Med Sci. 1981.
PMID: 7239878
No abstract available.
Item in Clipboard
Cite
Cite