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Mackinder's hereditary brachydactyly: phenotypic, radiological, dermatoglyphic and genetic observations in an Ontario family.

作者信息

Battle H I, Walker N F, Thompson M W

出版信息

Ann Hum Genet. 1973 Apr;36(4):415-24. doi: 10.1111/j.1469-1809.1973.tb00605.x.

DOI:10.1111/j.1469-1809.1973.tb00605.x
PMID:4748760
Abstract
摘要

相似文献

1
Mackinder's hereditary brachydactyly: phenotypic, radiological, dermatoglyphic and genetic observations in an Ontario family.麦金德遗传性短指畸形:安大略省一个家族的表型、放射学、皮纹学及遗传学观察
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The facio-audio-symphalangism syndrome: report of a case and review of the literature.面-听-并指综合征:1例报告及文献复习
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引用本文的文献

1
Brachydactyly type B: linkage to chromosome 9q22 and evidence for genetic heterogeneity.B型短指症:与9号染色体q22区域的连锁关系及遗传异质性证据
Am J Hum Genet. 1999 Feb;64(2):578-85. doi: 10.1086/302255.
2
Brachydactyly type B: clinical description, genetic mapping to chromosome 9q, and evidence for a shared ancestral mutation.B型短指症:临床描述、9号染色体长臂的基因定位及共同祖先突变的证据
Am J Hum Genet. 1999 Feb;64(2):570-7. doi: 10.1086/302249.
3
Hereditary brachydactyly with nail dysplasia.伴有指甲发育异常的遗传性短指症。
J Med Genet. 1979 Jun;16(3):236. doi: 10.1136/jmg.16.3.236.
4
Classification and identification of inherited brachydactylies.遗传性短指(趾)症的分类与鉴定
J Med Genet. 1979 Feb;16(1):36-44. doi: 10.1136/jmg.16.1.36.