✦ LIBER ✦

Restriction fragment length polymorphism of two HLA-B-associated transcripts genes in five autoimmune diseases

✍ Scribed by Fugger, L.; Morling, N.; Ryder, L.P.; Jakobsen, B.K.; Andersen, V.; Oxholm, P.; Dalhoff, Kim; Heilmann, C.; Karup Pedersen, F.; Friis, J.

Book ID: 123003058
Publisher: Elsevier Science
Year: 1991
Tongue: English
Weight: 290 KB
Volume: 30
Category: Article
ISSN: 0198-8859
DOI: 10.1016/0198-8859(91)90067-J

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Restriction fragment length polymorplusm

Restriction fragment length polymorplusm (RFLP) of two HLA-B-associated transcripts (BATS)- genes in healthy Danes

✍ L. Fugger; N. Morling; L. P. Ryder; B. K. Jakobsen; A. Svejgaard; T. Spies; J. L 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 414 KB

Restriction fragment length polymorphism

Restriction fragment length polymorphism in four virulence-associated genes of Listeria monocytogenes

✍ Vines, A.; Reeves, M.W.; Hunter, S.; Swaminathan, B. 📂 Article 📅 1992 🏛 Elsevier Science 🌐 English ⚖ 646 KB

Restriction fragment length polymorphism

Restriction fragment length polymorphism in HLA class II genes of Latin-American caucasian celiac disease patients

✍ Herrera, Mariana; Chertkoff, Lilien; Palavecino, Ethel; Mota, Alicia; del Carmen 📂 Article 📅 1989 🏛 Elsevier Science 🌐 English ⚖ 598 KB

Nco I Restriction Fragment Length Polymo

Nco I Restriction Fragment Length Polymorphism (RFLP) of the Tumor Necrosis Factor (TNFα) region in four autoimmune diseases

✍ L. Fugger; N. Morling; L. P. Ryder; J. Georgsen; B. K. Jakobsen; A. Svejgaard; V 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 275 KB

Restriction fragment length polymorphism

Restriction fragment length polymorphism (RFLP) analysis of class II MHC genes in SLE: Lack of disease association in american blacks

✍ Reveille, J.D.; Acton, R.T.; Barger, B.O. 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 79 KB

Defective, deleted or converted CYP21B g

Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia

✍ N. Ghanem; J. M. Lobaccaro; C. Buresi; M. Abbal; G. Halaby; C. Sultan; G. Lefran 📂 Article 📅 1990 🏛 Springer 🌐 English ⚖ 922 KB

Defects in the enzyme, steroid 21-hydroxylase, result in congenital adrenal hyperplasia (CAH), a common autosomal recessive disorder of cortisol biosynthesis. The gene encoding this protein (CYP21B) and a closely linked pseudogene (CYP21A) have been mapped in the HLA complex on chromosome 6p, adjace