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Page 1
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies.
Genet Med. 2016 Jun;18(6):554-62. doi: 10.1038/gim.2015.127. Epub 2015 Sep 10.
Genet Med. 2016.
PMID: 26355662
Free article.
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies.
Monies D, Alhindi HN, Almuhaizea MA, Abouelhoda M, Alazami AM, Goljan E, Alyounes B, Jaroudi D, AlIssa A, Alabdulrahman K, Subhani S, El-Kalioby M, Faquih T, Wakil SM, Altassan NA, Meyer BF, Bohlega S.
Monies D, et al.
Hum Genomics. 2016 Sep 27;10(1):32. doi: 10.1186/s40246-016-0089-8.
Hum Genomics. 2016.
PMID: 27671536
Free PMC article.
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Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection.
Mustafa AE, Faquih T, Baz B, Kattan R, Al-Issa A, Tahir AI, Imtiaz F, Ramzan K, Al-Sayed M, Alowain M, Al-Hassnan Z, Al-Zaidan H, Abouelhoda M, Al-Mubarak BR, Al Tassan NA.
Mustafa AE, et al. Among authors: al issa a.
Genes (Basel). 2018 May 22;9(5):267. doi: 10.3390/genes9050267.
Genes (Basel). 2018.
PMID: 29789446
Free PMC article.
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