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Year | Number of Results |
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1998 | 1 |
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2013 | 1 |
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PubMed (cited) for id: 300827
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Identification of a novel familial FGF16 mutation in metacarpal 4-5 fusion.
Clin Dysmorphol. 2014 Jul;23(3):95-97. doi: 10.1097/MCD.0000000000000043.
Clin Dysmorphol. 2014.
PMID: 24878828
No abstract available.
Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion.
Jamsheer A, Zemojtel T, Kolanczyk M, Stricker S, Hecht J, Krawitz P, Doelken SC, Glazar R, Socha M, Mundlos S.
Jamsheer A, et al.
J Med Genet. 2013 Sep;50(9):579-84. doi: 10.1136/jmedgenet-2013-101659. Epub 2013 May 24.
J Med Genet. 2013.
PMID: 23709756
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The human FGF gene family: chromosome location and phylogenetic analysis.
Kim HS.
Kim HS.
Cytogenet Cell Genet. 2001;93(1-2):131-2. doi: 10.1159/000056965.
Cytogenet Cell Genet. 2001.
PMID: 11474196
No abstract available.
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Structure and expression of a novel member, FGF-16, on the fibroblast growth factor family.
Miyake A, Konishi M, Martin FH, Hernday NA, Ozaki K, Yamamoto S, Mikami T, Arakawa T, Itoh N.
Miyake A, et al.
Biochem Biophys Res Commun. 1998 Feb 4;243(1):148-52. doi: 10.1006/bbrc.1998.8073.
Biochem Biophys Res Commun. 1998.
PMID: 9473496
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