Author:
Tsukahara Masato,Azuno Yoichi,Kajii Tadashi
Reference6 articles.
1. (1951): On brachydactyly and symphalangism. In (ed): “The Treasury of Human Inheritance.” London: Cambridge University Press, pp 1-31.
2. Classification and identification of inherited brachydactylies
3. Conductive deafness, symphalangism, and facial abnormalities: The WL syndrome in a Japanese family
4. (1988): “Mendelian Inheritance in Man. Catalogs of Autosomal Recessive and X-Linked Phenotypes.” Baltimore: The Johns Hopkins University Press, 8th Ed, p 109.
Cited by
15 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. The third patient with Tsukahara-Azuno-Kaiji syndrome with type A1 brachydactyly, dwarfism, microcephaly, scoliosis, intellectual disability, ptosis, and hearing loss;Radiology Case Reports;2022-01
2. Homozygous microdeletion of the ERI1
and MFHAS1
genes in a patient with intellectual disability, limb abnormalities, and cardiac malformation;American Journal of Medical Genetics Part A;2017-05-09
3. Intellectual disability, unusual facial morphology and hand anomalies in sibs;American Journal of Medical Genetics Part A;2013-08
4. How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?;American Journal of Medical Genetics Part A;2011-03-17
5. A second patient with Tsukahara syndrome: Type A1 brachydactyly, short stature, hearing loss, microcephaly, mental retardation and ptosis;American Journal of Medical Genetics Part A;2010-04