Trichorhinophalangeal syndrome type I and systemic lupus erythematosus with complement C4A homozygous null alleles in the same family.

Author:

Dahlqvist S R,Lundstrom B,Holmgren G

Publisher

BMJ

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Rheumatology

Reference13 articles.

1. Autosomaldominant transmission of the tricho-rhino-phalangeal syndrome. Report of 4 unrelated families, review of 60 cases;Giedion, A.; Burdea, M.; Meloni, Fruchter Z.; T.;Helv Paediatr Acta,1973

2. The tricho-rhinophalangeal syndrome;D, Weaver D.; M, Cohen; W, Smith D.;J Med Genet,1974

3. Peripheral dysostosis, acrodysostosis and Thiemann's disease;Acrocysplasias, Giedion A.;Clin Orthop,1976

4. Terminal or interstitial deletion;M, Buhler E.; K, Buihler U.; R, Clinsten

5. Trichorhinophalangeal syndrome type I: symptoms and signs, radiology and genetics;Noltorp, S.; Kristoffersson, U.; Mandahl, N.; Stigsson, L.; Svensson, B.; Werner, C.-O.;Ann Rheum Dis,1986

Cited by 1 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. Trichorhinophalangeal syndrome, type I;Journal of the American Academy of Dermatology;1994-08

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