Author:
Stamatoyannopoulos G.,Nute P. E.,Miller M.
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference22 articles.
1. Blank CE (1960) Apert's syndrome (a type of acrocephalosyndactyly) —observations on a British series of 39 cases. Ann Hum Genet 24: 151–164
2. Borberg A (1951) Clinical and genetic investigations into tuberous sclerosis and Recklinghausen's neurofibromatosis. Munksgaard, Copenhagen
3. Bunn HF, Bradley TB, Davis WE, Drysdale JW, Burke JF, Beck WS, Laver MB (1972) Structural and functional studies on hemoglobin Bethesda (a
2β
2
145His
), a variant associated with compensatory erythrocytosis. J Clin Invest 51:2299–2309
4. Bunn HF, Forget BG, Ranney HM (1977) Human hemoglobins. Saunders, Philadelphia
5. Erickson JD, Cohen MM (1974) A study of parental age effects on the occurrence of fresh mutations for the Apert syndrome. Ann Hum Genet 38:89–96
Cited by
13 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