Kruse TA - Search Results

1

Assignment of the urokinase-type plasminogen activator receptor gene (PLAUR) to chromosome 19q13.1-q13.2.

Børglum AD, Byskov A, Ragno P, Roldan AL, Tripputi P, Cassani G, Danø K, Blasi F, Bolund L, Kruse TA. Børglum AD, et al. Among authors: kruse ta. Am J Hum Genet. 1992 Mar;50(3):492-7. Am J Hum Genet. 1992. PMID: 1311495 Free PMC article.

2

Two PstI polymorphisms for the urokinase-type plasminogen activator receptor gene (PLAUR).

Børglum AD, Byskov A, Roldan AL, Kruse TA. Børglum AD, et al. Among authors: kruse ta. Hum Genet. 1992 Jul;89(5):584. doi: 10.1007/BF00219193. Hum Genet. 1992. PMID: 1353059

3

X-linked retinitis pigmentosa: new map studies of XLRP2, and a possible human centromere effect.

Friedrich U, Warburg M, Kruse TA, Andréasson S. Friedrich U, et al. Among authors: kruse ta. Hum Genet. 1992 Mar;88(6):683-7. doi: 10.1007/BF02265297. Hum Genet. 1992. PMID: 1551673

4

Multipoint linkage analysis in Menkes disease.

Tønnesen T, Petterson A, Kruse TA, Gerdes AM, Horn N. Tønnesen T, et al. Among authors: kruse ta. Am J Hum Genet. 1992 May;50(5):1012-7. Am J Hum Genet. 1992. PMID: 1570830 Free PMC article.

5

Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region.

Alitalo T, Kruse TA, Ahrens P, Albertsen HM, Eriksson AW, de la Chapelle A. Alitalo T, et al. Among authors: kruse ta. Hum Genet. 1991 Apr;86(6):599-603. doi: 10.1007/BF00201548. Hum Genet. 1991. PMID: 1673960

6

An EcoRI polymorphism for the PLAUR gene.

Børglum AD, Byskov A, Cubellis MV, Kruse TA. Børglum AD, et al. Among authors: kruse ta. Nucleic Acids Res. 1991 Dec 11;19(23):6661. doi: 10.1093/nar/19.23.6661-a. Nucleic Acids Res. 1991. PMID: 1684424 Free PMC article.

7

Multipoint linkage analysis in X-linked Alport syndrome.

Hertz JM, Kruse TA, Thomsen A, Spencer ES. Hertz JM, et al. Among authors: kruse ta. Hum Genet. 1991 Dec;88(2):157-61. doi: 10.1007/BF00206064. Hum Genet. 1991. PMID: 1684562

8

Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis.

Alitalo T, Kruse TA, Forsius H, Eriksson AW, de la Chapelle A. Alitalo T, et al. Among authors: kruse ta. Am J Hum Genet. 1991 Jan;48(1):31-8. Am J Hum Genet. 1991. PMID: 1985461 Free PMC article.

9

Female haemophilia A in a family with seeming extreme bidirectional lyonization tendency: abnormal premature X-chromosome inactivation?

Ingerslev J, Schwartz M, Lamm LU, Kruse TA, Bukh A, Stenbjerg S. Ingerslev J, et al. Among authors: kruse ta. Clin Genet. 1989 Jan;35(1):41-8. doi: 10.1111/j.1399-0004.1989.tb02903.x. Clin Genet. 1989. PMID: 2564325

10

Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12.

Kølvraa S, Kruse TA, Jensen PK, Linde KH, Vestergaard SR, Bolund L. Kølvraa S, et al. Among authors: kruse ta. Hum Genet. 1986 Nov;74(3):284-7. doi: 10.1007/BF00282550. Hum Genet. 1986. PMID: 2877938

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