Similar articles for PMID: 3793105

Year	Number of Results
1979	1
1981	2
1984	1
1985	4
1986	15
1987	19
1988	20
1989	16
1990	8
1991	3
1992	5
1993	1
1997	1
2024	0

1

Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14-q21.

Mattei MG, Colin Y, Le Van Kim C, Mattei JF, Cartron JP. Mattei MG, et al. Hum Genet. 1986 Dec;74(4):420-2. doi: 10.1007/BF00280497. Hum Genet. 1986. PMID: 3793105

2

Sublocalization of the human protein C gene on chromosome 2q13-q14.

Patracchini P, Aiello V, Palazzi P, Calzolari E, Bernardi F. Patracchini P, et al. Hum Genet. 1989 Jan;81(2):191-2. doi: 10.1007/BF00293902. Hum Genet. 1989. PMID: 2912888

3

Characterization of cDNA clones for human glycophorin A. Use for gene localization and for analysis of normal of glycophorin-A-deficient (Finnish type) genomic DNA.

Rahuel C, London J, d'Auriol L, Mattei MG, Tournamille C, Skrzynia C, Lebouc Y, Galibert F, Cartron JP. Rahuel C, et al. Eur J Biochem. 1988 Feb 15;172(1):147-53. doi: 10.1111/j.1432-1033.1988.tb13866.x. Eur J Biochem. 1988. PMID: 3345758 Free article.

4

Regional localization of the LCA oncogene to human chromosome region 2q14----q21.

Tokino T, Satoh H, Yoshida MC, Ochiya T, Matsubara K. Tokino T, et al. Cytogenet Cell Genet. 1988;48(1):63-4. doi: 10.1159/000132589. Cytogenet Cell Genet. 1988. PMID: 2846240

5

Structure of human erythrocyte glycophorin C deduced from cDNA analysis.

Cartron JP, Colin Y, Le Van Kim C, Rahuel C, Blanchard D, Bloy C, London J. Cartron JP, et al. Rev Fr Transfus Immunohematol. 1986 Sep;29(4):267-85. doi: 10.1016/s0338-4535(86)80020-4. Rev Fr Transfus Immunohematol. 1986. PMID: 3544149 Review. No abstract available.

6

RFLPs for the human erythrocyte membrane glycophorin C gene.

Arveiler B, Le Van Kim C, Colin Y, Mandel JL, Cartron JP. Arveiler B, et al. Nucleic Acids Res. 1987 Feb 25;15(4):1880. doi: 10.1093/nar/15.4.1880. Nucleic Acids Res. 1987. PMID: 2881278 Free PMC article. No abstract available.

7

Localization of the human Rh blood group gene structure to chromosome region 1p34.3-1p36.1 by in situ hybridization.

Chérif-Zahar B, Mattéi MG, Le Van Kim C, Bailly P, Cartron JP, Colin Y. Chérif-Zahar B, et al. Hum Genet. 1991 Feb;86(4):398-400. doi: 10.1007/BF00201843. Hum Genet. 1991. PMID: 1900257

8

Human gene coding for granulocyte-colony stimulating factor is assigned to the q21-q22 region of chromosome 17.

Kanda N, Fukushige S, Murotsu T, Yoshida MC, Tsuchiya M, Asano S, Kaziro Y, Nagata S. Kanda N, et al. Somat Cell Mol Genet. 1987 Nov;13(6):679-84. doi: 10.1007/BF01534488. Somat Cell Mol Genet. 1987. PMID: 3499671

9

De novo t(2;13)(p24.3;q14.2) and retinoblastoma. Mapping of two 13q14 probes by in situ hybridization.

Blanquet V, Turleau C, Créau-Goldberg N, Cochet C, de Grouchy J. Blanquet V, et al. Hum Genet. 1987 May;76(1):102-5. doi: 10.1007/BF00283059. Hum Genet. 1987. PMID: 3502693

10

Alteration of the genes for glycophorin A and B in glycophorin-A-deficient individuals.

Rahuel C, London J, Vignal A, Cherif-Zahar B, Colin Y, Siebert P, Fukuda M, Cartron JP. Rahuel C, et al. Eur J Biochem. 1988 Nov 15;177(3):605-14. doi: 10.1111/j.1432-1033.1988.tb14413.x. Eur J Biochem. 1988. PMID: 3197721 Free article.

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