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Items: 1 to 20 of 103

1.

Assignment of the human antithrombin III structural gene to chromosome 1q23-25.

Bock SC, Harris JF, Balazs I, Trent JM.

Cytogenet Cell Genet. 1985;39(1):67-9.

PMID:
3979120
2.

Genetic mapping of the structural gene for antithrombin III to human chromosome 1.

Kao FT, Morse HG, Law ML, Lidsky A, Chandra T, Woo SL.

Hum Genet. 1984;67(1):34-6.

PMID:
6086493
3.
4.

Cloning and expression of the cDNA for human antithrombin III.

Bock SC, Wion KL, Vehar GA, Lawn RM.

Nucleic Acids Res. 1982 Dec 20;10(24):8113-25.

5.

Confirmation of linkage between antithrombin III and Duffy blood group and assignment of AT3 to 1q22 lead to q25.

Winter JH, Bennett B, Watt JL, Brown T, San Román C, Schinzel A, King J, Cook PJ.

Ann Hum Genet. 1982 Jan 1;46(Pt 1):29-34. No abstract available.

PMID:
7103410
6.
7.

Isolation of a cDNA clone for human antithrombin III.

Prochownik EV, Markham AF, Orkin SH.

J Biol Chem. 1983 Jul 10;258(13):8389-94.

8.

A NheI RFLP in the human antithrombin III gene (1q23-q25) (AT3).

Bock SC, Radziejewska E.

Nucleic Acids Res. 1991 May 11;19(9):2519. No abstract available.

9.

A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency.

Pallotta R, Dalprà L, Miozzo M, Ehresmann T, Fusilli P.

Am J Med Genet. 2001 Dec 15;104(4):282-6.

PMID:
11754060
10.

Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1.

Magenis RE, Donlon T, Parks M, Rivas ML, Lovrien EW.

Cytogenet Cell Genet. 1978;22(1-6):327-9. No abstract available.

PMID:
752496
11.

Localization of human U1 small nuclear RNA genes to band p36.3 of chromosome 1 by in situ hybridization.

Naylor SL, Zabel BU, Manser T, Gesteland R, Sakaguchi AY.

Somat Cell Mol Genet. 1984 May;10(3):307-13.

PMID:
6202011
12.

Human platelet factor 4 gene is mapped to 4q12----q21.

Griffin CA, Emanuel BS, LaRocco P, Schwartz E, Poncz M.

Cytogenet Cell Genet. 1987;45(2):67-9.

PMID:
3622011
13.

Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23.

Roberts AG, Whatley SD, Daniels J, Holmans P, Fenton I, Owen MJ, Thompson P, Long C, Elder GH.

Hum Mol Genet. 1995 Dec;4(12):2387-90.

PMID:
8634714
14.

Assignment of a gene for succinate dehydrogenase to human chromosome 1 by somatic cell hybridization.

Mascarello JT, Soderberg K, Scheffler IE.

Cytogenet Cell Genet. 1980;28(1-2):121-35.

PMID:
6934864
15.

Localization of the human cystatin D gene (CST5) to chromosome 20p11.21 by in situ hybridization.

Freije JP, Pendás AM, Velasco G, Roca A, Abrahamson M, López-Otín C.

Cytogenet Cell Genet. 1993;62(1):29-31.

PMID:
8422752
16.

Assignment of the human homologue of the mTRiC-P5 gene (TRIC5) to band 1q23 by fluorescence in situ hybridization.

Sévigny G, Joly EC, Bibor-Hardy V, Lemieux N.

Genomics. 1994 Aug;22(3):634-6.

PMID:
8001976
17.

Chromosome localization of the gene for human terminal deoxynucleotidyltransferase to region 10q23-q25.

Isobe M, Huebner K, Erikson J, Peterson RC, Bollum FJ, Chang LM, Croce CM.

Proc Natl Acad Sci U S A. 1985 Sep;82(17):5836-40.

18.

Chromosomal localization of the human alpha 1-antitrypsin gene (PI) to 14q31-32.

Schroeder WT, Miller MF, Woo SL, Saunders GF.

Am J Hum Genet. 1985 Sep;37(5):868-72.

19.

Assignment of the human myeloperoxidase gene (MPO) to bands q21.3----q23 of chromosome 17.

Inazawa J, Inoue K, Nishigaki H, Tsuda S, Taniwaki M, Misawa S, Abe T.

Cytogenet Cell Genet. 1989;50(2-3):135-6.

PMID:
2550177
20.

The human gene for the beta subunit of nerve growth factor is located on the proximal short arm of chromosome 1.

Francke U, de Martinville B, Coussens L, Ullrich A.

Science. 1983 Dec 16;222(4629):1248-51.

PMID:
6648531

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