Mackinder's hereditary brachydactyly: phenotypic, radiological, dermatoglyphic and genetic observations in an Ontario family
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1973.tb00605.x/fullpdf
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1. CONGENITAL HEREDITARY ABSENCE OF SOME OF THE DIGITAL PHALANGES
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B;Nature Genetics;2000-03
2. Brachydactyly Type B: Linkage to Chromosome 9q22 and Evidence for Genetic Heterogeneity;The American Journal of Human Genetics;1999-02
3. Brachydactyly Type B: Clinical Description, Genetic Mapping to Chromosome 9q, and Evidence for a Shared Ancestral Mutation;The American Journal of Human Genetics;1999-02
4. Septo-optic dysplasia with digital anomalies;The Journal of Pediatrics;1984-12
5. Hereditary brachydactyly with nail dysplasia.;Journal of Medical Genetics;1979-06-01
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