A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders
2005 ◽
Vol 115
(5)
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pp. 1250-1257
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Keyword(s):
1995 ◽
Vol 59
(2)
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pp. 134-138
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Keyword(s):
1997 ◽
Vol 17
(8)
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pp. 773-776
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2016 ◽
Vol 32
(4)
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pp. 338-341
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2005 ◽
Vol 53
(1)
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pp. S272.4-S272
2013 ◽
Vol 71
(7)
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pp. 1195-1201
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