Bender K - Search Results

1

Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17.

Koch MC, Ricker K, Otto M, Grimm T, Hoffman EP, Rüdel R, Bender K, Zoll B, Harper PS, Lehmann-Horn F. Koch MC, et al. Among authors: bender k. J Med Genet. 1991 Sep;28(9):583-6. doi: 10.1136/jmg.28.9.583. J Med Genet. 1991. PMID: 1683408 Free PMC article.

2

Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.

Koch MC, Ricker K, Otto M, Grimm T, Bender K, Zoll B, Harper PS, Lehmann-Horn F, Rüdel R, Hoffman EP. Koch MC, et al. Among authors: bender k. Hum Genet. 1991 Nov;88(1):71-4. doi: 10.1007/BF00204932. Hum Genet. 1991. PMID: 1660029

3

A linkage study of malignant hyperthermia (MH).

Bender K, Senff H, Wienker TF, Spiess-Kiefer C, Lehmann-Horn F. Bender K, et al. Clin Genet. 1990 Mar;37(3):221-5. doi: 10.1111/j.1399-0004.1990.tb03506.x. Clin Genet. 1990. PMID: 2323092

4

Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19.

Koch M, Harley H, Sarfarazi M, Bender K, Wienker T, Zoll B, Harper PS. Koch M, et al. Among authors: bender k. Hum Genet. 1989 May;82(2):163-6. doi: 10.1007/BF00284051. Hum Genet. 1989. PMID: 2722193

5

Linkage studies of Myotonia congenita and Paramyotonia congenita.

Bender K, Senff H, Steiert A, Lagodny H, Wienker TF, Koch M. Bender K, et al. Clin Genet. 1989 Aug;36(2):92-9. doi: 10.1111/j.1399-0004.1989.tb03170.x. Clin Genet. 1989. PMID: 2766573

6

Linkage relations of JK, CO, KEL and IGK with each other and with AHCY.

Bender K, Bissbort S, Crone H, Senff H, Steiert A, Neumann H, Koch M, Nagel M, Wienker TF. Bender K, et al. Hum Hered. 1988;38(1):12-7. doi: 10.1159/000153747. Hum Hered. 1988. PMID: 3127321

7

New mutation to Huntington's disease.

Wolff G, Deuschl G, Wienker TF, Hummel K, Bender K, Lücking CH, Schumacher M, Hammer J, Oepen G. Wolff G, et al. Among authors: bender k. J Med Genet. 1989 Jan;26(1):18-27. doi: 10.1136/jmg.26.1.18. J Med Genet. 1989. PMID: 2563774 Free PMC article.

8

Evidence for preferential X-chromosome inactivation in a family with Fabry disease.

Ropers HH, Wienker TF, Grimm T, Schroetter K, Bender K. Ropers HH, et al. Among authors: bender k. Am J Hum Genet. 1977 Jul;29(4):361-70. Am J Hum Genet. 1977. PMID: 406783 Free PMC article.

9

Linkage between the variegate porphyria (VP) and the alpha-1-antitrypsin (PI) genes on human chromosome 14.

Bissbort S, Hitzeroth HW, du Wentzel DP, Van den Berg CW, Senff H, Wienker TF, Bender K. Bissbort S, et al. Among authors: bender k. Hum Genet. 1988 Jul;79(3):289-90. doi: 10.1007/BF00366255. Hum Genet. 1988. PMID: 3261272

10

Biochemical genetics of methylglyoxal dehydrogenases in the laboratory rat (Rattus norvegicus).

Bender K, Seibert RT, Wienker TF, Kren V, Pravenec M, Bissbort S. Bender K, et al. Biochem Genet. 1994 Jun;32(5-6):147-54. doi: 10.1007/BF00554618. Biochem Genet. 1994. PMID: 7993370

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