Similar articles for PMID: 2563250

Year	Number of Results
1979	1
1980	1
1981	2
1982	2
1983	1
1984	5
1985	7
1986	8
1987	18
1988	27
1989	28
1990	25
1991	19
1992	15
1993	7
1994	7
1995	2
1996	2
1999	1
2000	1
2001	1
2007	1
2008	1
2009	1
2024	0

1

Localization of the coagulation factor XIII B subunit gene (F13B) to chromosome bands 1q31-32.1 and restriction fragment length polymorphism at the locus.

Webb GC, Coggan M, Ichinose A, Board PG. Webb GC, et al. Hum Genet. 1989 Jan;81(2):157-60. doi: 10.1007/BF00293893. Hum Genet. 1989. PMID: 2563250

2

The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies.

Wu JS, Giuffra LA, Goodfellow PJ, Myers S, Carson NL, Anderson L, Hoyle LS, Simpson NE, Kidd KK. Wu JS, et al. Hum Genet. 1989 Nov;83(4):383-90. doi: 10.1007/BF00291386. Hum Genet. 1989. PMID: 2572537

3

Localization of the coagulation factor XIII A subunit gene (F13A) to chromosome bands 6p24----p25.

Board PG, Webb GC, McKee J, Ichinose A. Board PG, et al. Cytogenet Cell Genet. 1988;48(1):25-7. doi: 10.1159/000132580. Cytogenet Cell Genet. 1988. PMID: 2903011

4

Haplotypes of the coagulation factor XIII A subunit locus in normal and deficient subjects.

Board PG, Chapple R, Coggan M. Board PG, et al. Am J Hum Genet. 1988 May;42(5):712-7. Am J Hum Genet. 1988. PMID: 2895980 Free PMC article.

5

Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA.

Zoghbi HY, Daiger SP, McCall A, O'Brien WE, Beaudet AL. Zoghbi HY, et al. Am J Hum Genet. 1988 Jun;42(6):877-83. Am J Hum Genet. 1988. PMID: 2897163 Free PMC article.

6

The anonymous PAS45 probe detects RFLPs in 13q31.

Gross MS, Sefiani A, de Tand MF, Lau YF, Saidi-Mehtar N, Hors-Cayla MC, Frezal J, Van Cong N. Gross MS, et al. Ann Genet. 1989;32(2):73-7. Ann Genet. 1989. PMID: 2569289

7

The gene encoding human low-molecular weight insulin-like growth-factor binding protein (IGF-BP25): regional localization to 7p12-p13 and description of a DNA polymorphism.

Alitalo T, Kontula K, Koistinen R, Aalto-Setälä K, Julkunen M, Jänne OA, Seppälä M, de la Chapelle A. Alitalo T, et al. Hum Genet. 1989 Nov;83(4):335-8. doi: 10.1007/BF00291377. Hum Genet. 1989. PMID: 2478445

8

Chromosomal localization of human aspartate aminotransferase genes by in situ hybridization.

Pol S, Bousquet-Lemercier B, Pavé-Preux M, Bulle F, Passage E, Hanoune J, Mattei MG, Barouki R. Pol S, et al. Hum Genet. 1989 Sep;83(2):159-64. doi: 10.1007/BF00286710. Hum Genet. 1989. PMID: 2777255

9

The X chromosome shows less genetic variation at restriction sites than the autosomes.

Hofker MH, Skraastad MI, Bergen AA, Wapenaar MC, Bakker E, Millington-Ward A, van Ommen GJ, Pearson PL. Hofker MH, et al. Am J Hum Genet. 1986 Oct;39(4):438-51. Am J Hum Genet. 1986. PMID: 2876629 Free PMC article.

10

Restriction fragment length polymorphisms detected by anonymous DNA probes mapped to defined intervals of human chromosome 16.

Hyland VJ, Grist S, Sutherland GR. Hyland VJ, et al. Hum Genet. 1988 Jul;79(3):277-9. doi: 10.1007/BF00366251. Hum Genet. 1988. PMID: 2900214

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