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A. Schinzel, W. Schmid (1980)
Interstitial deletion of the long arm of chromosome 1, del(1)(q21‐q25) in a profoundly retarded 8‐year‐old girl with multiple anomaliesClinical Genetics, 18
Magenis Magenis, Donlon Donlon, Parks Parks, Rivas Rivas, Lovrien Lovrien (1978)
Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1Human Gene Mapping, 4
Meyers Meyers, Merritt Merritt, Conneally Conneally, Norton Norton, Rivas Rivas, Yu Yu, Palmer Palmer (1978)
Linkage group I: a statistically significant locus order from family studiesHuman Gene Mapping, 4
Bishop Bishop, Baty Baty, Martin Martin, Cosgriff Cosgriff, Skolnick Skolnick, Hasstedt Hasstedt, Hershgold Hershgold (1979)
Heterogeneity in antithrombin III deficiency. Linkage to chromosome 1 and chromosome 6Am. J. Hum. Genet., 31
Bishop Bishop, Skolnick Skolnick, Baty Baty, Cosgriff Cosgriff, Martin Martin, Hershgold Hershgold (1981)
Linkage of familial antithrombin III deficiency to DuffyHuman Gene Mapping, 6
R. Palmer, M. Hultén (1982)
Chiasma derived genetic maps and recombination fractions: chromosome 13 with reference to the proposed 13q14 retinoblastoma locus.Journal of Medical Genetics, 19
M. Mackie, B. Bennett, D. Ogston, A. Douglas (1978)
Familial thrombosis: inherited deficiency of antithrombin III.British Medical Journal, 1
Hultén Hultén, Palmer Palmer, Laurie Laurie (1981)
Chiasma derived male genetic maps and recombination fractions: chromosome 1Human Gene Mapping, 6
A. Sumner (1972)
A simple technique for demonstrating centromeric heterochromatin.Experimental cell research, 75 1
Ulrich Abildgaard, M. Lie, O. Ødegård (1977)
Antithrombin (heparin cofactor) assay with "new" chromogenic substrates (S-2238 and Chromozym TH).Thrombosis research, 11 4
Interstitial deletion in the long arms of chromosome 1:
Pablo Pablo, García Sagredo García Sagredo, Ferro Ferro, Ferrando Ferrando, San Román San Román (1980)
Interstitial deletion in the long arms of chromosome 1: 46, XY, del(1)(qter → q22::q25 → qter)J. Med. Genet., 17
(1978)
Linkage study of antithrombin 111
Human Gene Mapping, 6
J. Winter, A. Fenech, B. Bennett, A. Douglas (1981)
Transfusion Studies in Patients with Familial Antithrombin III (ATIII) Deficiency: Half‐disappearance Time of Infused ATIII and Influence of such Infusion on Platelet Life‐spanBritish Journal of Haematology, 49
antithrombin I11 deficiency to Duffy blood group
Heterogeneity in antithrombin 111 deficiency
J. Martsolf, M. Ray (1983)
Interstitial deletion of the long arm of chromosome 3.Annales de genetique, 26 2
D. Meyers, A. Merritt, P. Conneally, J. Norton, M. Rivas, P. Yu, C. Palmer (1978)
Linkage group I: a statistically significant locus order from family studies.Cytogenetics and cell genetics, 22 1-6
R. Magenis, T. Donlon, M. Parks, M. Rivas, E. Lovrien (1978)
Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1.Cytogenetics and cell genetics, 22 1-6
Lovrien Lovrien, Magenis Magenis, Rivas Rivas, Goodnight Goodnight, Moreland Moreland, Rowe Rowe (1978)
Linkage study of antithrombin IIIHuman Gene Mapping, 4
Bishop Bishop, Martin Martin, Baty Baty, Cosgriff Cosgriff, Hershgold Hershgold, Skolnick Skolnick (1978)
Linkage of antithrombin III deficiency to Duffy blood groupAm. J. Hum. Genet., 30
Human Gene Mapping, 5
SUMMARY Linkage studies on two families segregating for antithrombin III deficiency confirm the linkage between AT3 and the Duffy blood group. The maximum lod score including two published families is +4.2 at recombination fractions around 0.1. Two patients with deletions of 1q have 1/2 levels of antithrombin III suggesting that the AT3 locus lies in bands 1 q22 → 1q25.
Annals of Human Genetics – Wiley
Published: Jan 1, 1982
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