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Year | Number of Results |
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2000 | 2 |
2001 | 1 |
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2016 | 1 |
2024 | 0 |
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Page 1
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.
Nat Genet. 2016 Sep;48(9):1071-6. doi: 10.1038/ng.3592. Epub 2016 Jul 18.
Nat Genet. 2016.
PMID: 27428751
Free PMC article.
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.
Brancati F, Barrano G, Silhavy JL, Marsh SE, Travaglini L, Bielas SL, Amorini M, Zablocka D, Kayserili H, Al-Gazali L, Bertini E, Boltshauser E, D'Hooghe M, Fazzi E, Fenerci EY, Hennekam RC, Kiss A, Lees MM, Marco E, Phadke SR, Rigoli L, Romano S, Salpietro CD, Sherr EH, Signorini S, Stromme P, Stuart B, Sztriha L, Viskochil DH, Yuksel A, Dallapiccola B; International JSRD Study Group; Valente EM, Gleeson JG.
Brancati F, et al. Among authors: fenerci ey.
Am J Hum Genet. 2007 Jul;81(1):104-13. doi: 10.1086/519026. Epub 2007 May 18.
Am J Hum Genet. 2007.
PMID: 17564967
Free PMC article.
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Rare etiology of autosomal recessive disease in a child with noncarrier parents.
Lebo RV, Shapiro LR, Fenerci EY, Hoover JM, Chuang JL, Chuang DT, Kronn DF.
Lebo RV, et al. Among authors: fenerci ey.
Am J Hum Genet. 2000 Sep;67(3):750-4. doi: 10.1086/303042. Epub 2000 Jul 27.
Am J Hum Genet. 2000.
PMID: 10915611
Free PMC article.
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Joubert syndrome co-existing with partial Xp trisomy: review of the literature.
Güven GS, Fenerci EY, Deviren A, Ozkiliç A, Yüksel A, Hacihanefioğlu S.
Güven GS, et al. Among authors: fenerci ey.
Genet Couns. 2004;15(3):321-8.
Genet Couns. 2004.
PMID: 15517825
Review.
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Polymorphism analysis in the COLIA1 gene of patients with thalassemia major and intermedia.
Arisal O, Deviren A, Fenerci EY, Hacihanefioglu S, Ulutin T, Erkmen S, Buyru N.
Arisal O, et al. Among authors: fenerci ey.
Haematologia (Budap). 2002;32(4):475-82.
Haematologia (Budap). 2002.
PMID: 12803121
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Highly polymorphic short tandem repeat analyses clarify complex molecular test results.
Lebo RV, Maher T, Farrer L, Fenerci EY, Milunsky JM.
Lebo RV, et al. Among authors: fenerci ey.
Diagn Mol Pathol. 2001 Sep;10(3):179-89. doi: 10.1097/00019606-200109000-00006.
Diagn Mol Pathol. 2001.
PMID: 11552721
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Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.
Wyandt HE, Lebo RV, Fenerci EY, Sadhu DN, Milunsky JM.
Wyandt HE, et al. Among authors: fenerci ey.
Am J Med Genet. 2000 Aug 14;93(4):305-12.
Am J Med Genet. 2000.
PMID: 10946358
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