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Results: 1 to 20 of 119

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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
3.

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.

PMID:
1675011
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Interstitial deletion of chromosome 1q [del(1)(q24q25.3)] identified by fluorescence in situ hybridization and gene dosage analysis of apolipoprotein A-II, coagulation factor V, and antithrombin III.

Takano T, Yamanouchi Y, Mori Y, Kudo S, Nakayama T, Sugiura M, Hashira S, Abe T.

Am J Med Genet. 1997 Jan 20;68(2):207-10.

PMID:
9028459
[PubMed - indexed for MEDLINE]
5.

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.

PMID:
6298709
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

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
[PubMed - indexed for MEDLINE]
7.

Molecular genetic survey of 16 kindreds with hereditary antithrombin III deficiency.

Bock SC, Prochownik EV.

Blood. 1987 Nov;70(5):1273-8.

PMID:
3663935
[PubMed - indexed for MEDLINE]
Free Article
8.

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.

PMID:
6305982
[PubMed - indexed for MEDLINE]
Free Article
9.

Hereditary thrombosis in a Utah kindred is caused by a dysfunctional antithrombin III gene.

Bock SC, Harris JF, Schwartz CE, Ward JH, Hershgold EJ, Skolnick MH.

Am J Hum Genet. 1985 Jan;37(1):32-41.

PMID:
2983542
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

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
[PubMed - indexed for MEDLINE]
11.

Regional chromosome mapping of human collagen genes alpha 2(I) and alpha 1(I) (COLIA2 and COLIA1).

Retief E, Parker MI, Retief AE.

Hum Genet. 1985;69(4):304-8.

PMID:
3857213
[PubMed - indexed for MEDLINE]
12.

Localization of the thyroglobulin gene by in situ hybridization to human chromosomes.

Bergé-Lefranc JL, Cartouzou G, Mattéi MG, Passage E, Malezet-Desmoulins C, Lissitzky S.

Hum Genet. 1985;69(1):28-31.

PMID:
3967888
[PubMed - indexed for MEDLINE]
13.

Localization of the human progesterone receptor gene to chromosome 11q22-q23.

Rousseau-Merck MF, Misrahi M, Loosfelt H, Milgrom E, Berger R.

Hum Genet. 1987 Nov;77(3):280-2.

PMID:
3679212
[PubMed - indexed for MEDLINE]
14.

Chromosomal sublocalization of the human p97 melanoma antigen.

Le Beau MM, Diaz MO, Plowman GD, Brown JP, Rowley JD.

Hum Genet. 1986 Apr;72(4):294-6.

PMID:
3754536
[PubMed - indexed for MEDLINE]
15.

Mapping of human thyroglobulin gene on the long arm of chromosome 8 by in situ hybridization.

Avvedimento VE, Di Lauro R, Monticelli A, Bernardi F, Patracchini P, Calzolari E, Martini G, Varrone S.

Hum Genet. 1985;71(2):163-6.

PMID:
4043966
[PubMed - indexed for MEDLINE]
16.

Characterization of an unusual DNA length polymorphism 5' to the human antithrombin III gene.

Bock SC, Levitan DJ.

Nucleic Acids Res. 1983 Dec 20;11(24):8569-82.

PMID:
6672771
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

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
[PubMed - indexed for MEDLINE]
18.

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
[PubMed - indexed for MEDLINE]
19.

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
[PubMed - indexed for MEDLINE]
20.

Structure and chromosomal assignment of the sterol 12alpha-hydroxylase gene (CYP8B1) in human and mouse: eukaryotic cytochrome P-450 gene devoid of introns.

Gåfvels M, Olin M, Chowdhary BP, Raudsepp T, Andersson U, Persson B, Jansson M, Björkhem I, Eggertsen G.

Genomics. 1999 Mar 1;56(2):184-96.

PMID:
10051404
[PubMed - indexed for MEDLINE]

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