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Skeletal hand charts in inherited connective tissue disease.

作者信息

Parish J G

出版信息

J Med Genet. 1967 Dec;4(4):227-38. doi: 10.1136/jmg.4.4.227.

Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/f82ad8ec6aa0/jmedgene00383-0007-a.jpg

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本文引用的文献

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URINARY HYDROXYPROLINE EXCRETION IN MARFAN'S SYNDROME AS COMPARED WITH AGE MATCHED CONTROLS.
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FAMILIAL STREBLODACTLY WITH AMINO-ACIDURIA.伴有氨基酸尿症的家族性指(趾)细长症
Br Med J. 1963 Nov 16;2(5367):1247-50. doi: 10.1136/bmj.2.5367.1247.
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Marfan's syndrome and the Weill-Marchesani syndrome in the S. family.
Ann Intern Med. 1959 Nov;51:1049-70. doi: 10.7326/0003-4819-51-5-1049.
7
Marfan's syndrome in Northern Ireland; an account of thirteen families.
Ann Hum Genet. 1958 Jul;22(4):289-309. doi: 10.1111/j.1469-1809.1958.tb01423.x.
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