Johnson KJ - Search Results

1

Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20.

Sander T, Hildmann T, Wienker TF, Ramel C, Beck-Mannagetta G, Bianchi A, Sailer U, Berek K, Bauer G, Neitzel H, Schmitz B, Durner M, Johnson KJ, Janz D. Sander T, et al. Among authors: johnson kj. Am J Med Genet. 1996 Feb 16;67(1):31-9. doi: 10.1002/(SICI)1096-8628(19960216)67:1<31::AID-AJMG5>3.0.CO;2-V. Am J Med Genet. 1996. PMID: 8678111

2

Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5.

Sander T, Hildmann T, Janz D, Wienker TF, Bianchi A, Bauer G, Sailer U, Scaramelli A, Neitzel H, Schmitz B, Bailey ME, Beck-Mannagetta G, Johnson KJ, Darlison MG. Sander T, et al. Among authors: johnson kj. Epilepsy Res. 1996 Apr;23(3):235-44. doi: 10.1016/0920-1211(95)00098-4. Epilepsy Res. 1996. PMID: 8739126

3

Confirmation of the localization of the human GABAA receptor alpha 1-subunit gene (GABRA1) to distal 5q by linkage analysis.

Johnson KJ, Sander T, Hicks AA, van Marle A, Janz D, Mullan MJ, Riley BP, Darlison MG. Johnson KJ, et al. Genomics. 1992 Nov;14(3):745-8. doi: 10.1016/s0888-7543(05)80178-8. Genomics. 1992. PMID: 1330891

4

D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q.

Tsilfidis C, MacKenzie AE, Shutler G, Leblond S, Bailly J, Johnson K, Williamson R, Siegel-Bartelt J, Korneluk RG, Shelbourne P. Tsilfidis C, et al. Am J Hum Genet. 1991 Nov;49(5):961-5. Am J Hum Genet. 1991. PMID: 1928101 Free PMC article.

5

Direct molecular analysis of myotonic dystrophy in the German population: important considerations in genetic counselling.

Meiner A, Wolf C, Carey N, Okitsu A, Johnson K, Shelbourne P, Kunath B, Sauermann W, Thiele H, Kupferling P, et al. Meiner A, et al. J Med Genet. 1995 Aug;32(8):645-9. doi: 10.1136/jmg.32.8.645. J Med Genet. 1995. PMID: 7473660 Free PMC article.

6

A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.

Johnson K, Shelbourne P, Davies J, Buxton J, Nimmo E, Siciliano MJ, Bachinski LL, Anvret M, Harley H, Rundle S, et al. Johnson K, et al. Am J Hum Genet. 1990 Jun;46(6):1073-81. Am J Hum Genet. 1990. PMID: 1971149 Free PMC article.

7

Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers.

Lavedan C, Hofmann H, Shelbourne P, Duros C, Savoy D, Johnson K, Junien C. Lavedan C, et al. J Med Genet. 1991 Feb;28(2):89-91. doi: 10.1136/jmg.28.2.89. J Med Genet. 1991. PMID: 2002492 Free PMC article.

8

Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.

Johnson K, Nimmo E, Jones P, Weiss M, Savontaus ML, Anvret M, Bartlett R, Roses A, Shaw D, Harper PS, et al. Johnson K, et al. Hum Genet. 1988 Dec;80(4):379-81. doi: 10.1007/BF00273655. Hum Genet. 1988. PMID: 3198115

9

Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy.

Johnson KJ, Jones PJ, Spurr N, Nimmo E, Davies J, Creed H, Weiss M, Williamson R. Johnson KJ, et al. Cytogenet Cell Genet. 1988;48(1):13-5. doi: 10.1159/000132577. Cytogenet Cell Genet. 1988. PMID: 2460293

10

Comparison of CTG repeat length expansion and clinical progression of myotonic dystrophy over a five year period.

Martorell L, Martinez JM, Carey N, Johnson K, Baiget M. Martorell L, et al. J Med Genet. 1995 Aug;32(8):593-6. doi: 10.1136/jmg.32.8.593. J Med Genet. 1995. PMID: 7473648 Free PMC article.

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