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2015 | 1 |
2020 | 1 |
2024 | 0 |
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Identification and Characterization of BTD Gene Mutations in Jordanian Children with Biotinidase Deficiency.
J Pers Med. 2020 Jan 21;10(1):4. doi: 10.3390/jpm10010004.
J Pers Med. 2020.
PMID: 31973013
Free PMC article.
Two novel mutations of FBN1 in Jordanian patients with Marfan syndrome.
Jaradat SA, Abujamous LA, Al-Hawamdeh AA, Alawneh KM, Rawashdeh TA, Jaradat ZM.
Jaradat SA, et al. Among authors: jaradat zm.
Int J Clin Exp Med. 2015 Oct 15;8(10):18786-92. eCollection 2015.
Int J Clin Exp Med. 2015.
PMID: 26770496
Free PMC article.
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