Badarneh K - Search Results

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Comparative screening of FMF mutations in various communities of the Israeli society.

Sharkia R, Mahajnah M, Zalan A, Athamna M, Azem A, Badarneh K, Faris F. Sharkia R, et al. Among authors: badarneh k. Eur J Med Genet. 2013 Jul;56(7):351-5. doi: 10.1016/j.ejmg.2013.04.002. Epub 2013 Apr 18. Eur J Med Genet. 2013. PMID: 23602951

Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?

Fares F, Badarneh K, Abosaleh M, Harari-Shaham A, Diukman R, David M. Fares F, et al. Among authors: badarneh k. Prenat Diagn. 2008 Mar;28(3):236-41. doi: 10.1002/pd.1943. Prenat Diagn. 2008. PMID: 18264947

Whole-Exome Sequencing Identifies a Novel Homozygous Frameshift Mutation in the MTMR2 Gene as a Causative Mutation in a Patient with Charcot-Marie-Tooth Disease Type 4B1.

Abdalla-Moady T, Peleg A, Sadeh O, Badarneh K, Fares F. Abdalla-Moady T, et al. Among authors: badarneh k. Mol Neurobiol. 2018 Apr;55(4):3546-3550. doi: 10.1007/s12035-017-0588-1. Epub 2017 May 16. Mol Neurobiol. 2018. PMID: 28509084

Mutations in CYP11B1 and congenital adrenal hyperplasia in Moroccan Jews.

Paperna T, Gershoni-Baruch R, Badarneh K, Kasinetz L, Hochberg Z. Paperna T, et al. Among authors: badarneh k. J Clin Endocrinol Metab. 2005 Sep;90(9):5463-5. doi: 10.1210/jc.2005-1145. Epub 2005 Jul 19. J Clin Endocrinol Metab. 2005. PMID: 16030166

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