Author:
Svensson Elisabeth,von Döbeln Ulrika,Hagenfeldt Lars
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference28 articles.
1. Aulehla-Scholz C, Vorgerd M, Sautter E, Leupold D, Maulmann R, Ullrich K, Olek K, Horst J (1988) Phenylketonuria: distribution of DNA diagnostic patterns in German families. Hum Genet 78:353?355
2. Bergerheim U, Nordenskjöld M, Collins P (1989) Deletion mapping in renal cell carcinoma. Cancer Res 49:1390?1396
3. Chakraborty R, Lidsky AS, Daiger SP, Güttler F, Sullivan S, Di Lella AG, Woo SLC (1987) Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria. Hum Genet 76:40?46
4. Chen S-H, Hsiao K-J, Lin L-H, Liu T-T, Tang R-B, Su T-S (1989) Study of restriction fragment length polymorphisms at the human phenylalanine hydroxylase locus and evaluation of its potential application in prenatal diagnosis of phenylketonuria in Chinese. Hum Genet 81:226?230
5. Daiger SP, Chakraborty R, Güttler F, Lidsky AS, Koch R, Woo SLC (1986) Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuria. Lancet I:229?232
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