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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.

DOI:10.1136/jmg.4.4.227
PMID:6082898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1468561/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/b14ea47e278e/jmedgene00383-0011-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/f82ad8ec6aa0/jmedgene00383-0007-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/681c4ae1fe96/jmedgene00383-0008-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/d9ab301aeef8/jmedgene00383-0010-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/49e0884e4c9f/jmedgene00383-0010-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/b14ea47e278e/jmedgene00383-0011-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/f82ad8ec6aa0/jmedgene00383-0007-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/681c4ae1fe96/jmedgene00383-0008-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/d9ab301aeef8/jmedgene00383-0010-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/49e0884e4c9f/jmedgene00383-0010-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/1468561/b14ea47e278e/jmedgene00383-0011-a.jpg

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Skeletal hand charts in inherited connective tissue disease.遗传性结缔组织病中的手部骨骼图表。
J Med Genet. 1967 Dec;4(4):227-38. doi: 10.1136/jmg.4.4.227.
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引用本文的文献

1
The radiological features of a new bone dysplasia.一种新型骨发育异常的放射学特征。
Pediatr Radiol. 1981;11(2):109-13. doi: 10.1007/BF00971792.
2
Metacarpophalangeal pattern profile analysis in clinical genetics: an applied anthropometric method.临床遗传学中的掌指纹型分析：一种应用人体测量学方法
Am J Phys Anthropol. 1986 Jun;70(2):195-201. doi: 10.1002/ajpa.1330700206.
3
The metacarpal index--obsolete in Marfan syndrome!
Skeletal Radiol. 1992;21(6):371-4. doi: 10.1007/BF00241815.

本文引用的文献

1
Skeletal syndromes associated with arachnodactyly.与蜘蛛指（趾）相关的骨骼综合征。
Proc R Soc Med. 1960 Jul;53:515-8.
2
Osteochondrodystrophy (Morquio's disease) in three generations.三代人中的骨软骨发育不良（莫尔基奥氏病）
Lancet. 1959 Sep 26;2(7100):430-2. doi: 10.1016/s0140-6736(59)90418-0.
3
URINARY HYDROXYPROLINE EXCRETION IN MARFAN'S SYNDROME AS COMPARED WITH AGE MATCHED CONTROLS.
Proc Soc Exp Biol Med. 1964 Aug-Sep;116:931-3. doi: 10.3181/00379727-116-29412.
4
Marfan syndrome with coronary artery lesions in a North American Indian.一名北美印第安人患马凡综合征并伴有冠状动脉病变
Can Med Assoc J. 1976 Oct 9;115(7):651-3.
4
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.
5
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.
6
The Marfan syndrome: report of one case with autopsy, special histological study, and review of the literature.马方综合征：一例尸检、特殊组织学研究及文献复习报告
AMA Arch Intern Med. 1959 Jan;103(1):123-32. doi: 10.1001/archinte.1959.00270010129017.
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.
8
Causes of malformations of the heart.心脏畸形的病因。
Br Med J. 1965 Oct 16;2(5467):895-904. doi: 10.1136/bmj.2.5467.895.