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Year | Number of Results |
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2003 | 1 |
2013 | 1 |
2016 | 2 |
2024 | 0 |
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Page 1
Deep dermatophytosis and inherited CARD9 deficiency.
N Engl J Med. 2013 Oct 31;369(18):1704-1714. doi: 10.1056/NEJMoa1208487. Epub 2013 Oct 16.
N Engl J Med. 2013.
PMID: 24131138
Free PMC article.
Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage.
Belkadi A, Pedergnana V, Cobat A, Itan Y, Vincent QB, Abhyankar A, Shang L, El Baghdadi J, Bousfiha A; Exome/Array Consortium; Alcais A, Boisson B, Casanova JL, Abel L.
Belkadi A, et al.
Proc Natl Acad Sci U S A. 2016 Jun 14;113(24):6713-8. doi: 10.1073/pnas.1606460113. Epub 2016 May 31.
Proc Natl Acad Sci U S A. 2016.
PMID: 27247391
Free PMC article.
Clinical Trial.
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Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.
Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB, Belkadi A, Boisson B, Abel L, Clark AG; Greater Middle East Variome Consortium; Alkuraya FS, Casanova JL, Gleeson JG.
Scott EM, et al.
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.
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[KID syndrome: a cause of pachydermatoglyphia].
Stambouli OB, Belbachir A.
Stambouli OB, et al.
Ann Dermatol Venereol. 2003 Dec;130(12 Pt 1):1143-5.
Ann Dermatol Venereol. 2003.
PMID: 14724518
French.
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