Works matching IS 00015652 AND DT 1980 AND VI 30 AND IP 1

Results: 15

Alpha-1-Antitrypsin Phenotypes in French Canadian Newborns.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 1, doi. 10.1159/000153078

By:

Joly, J.;
Richer, G.;
Boisvert, F.;
Laverdière, M.

Publication type:

Article

Survey on Haemoglobin Variants, β-Thalassaemia, Glucose-6-Phosphate Dehydrogenase Deficiency and Haptoglobin Types in Turkish People Living in Manavgat, Serik and Boztepe (Antalya).

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 3, doi. 10.1159/000153079

By:

Aksoy, M.;
Dinçol, Günçağ;
Erdem, Şakir

Publication type:

Article

Interaction of Sickle Cell Trait and Glucose-6-Phosphate Dehydrogenase Deficiency in Cameroon.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 7, doi. 10.1159/000153080

By:

Bernstein, Shelly C.;
Bowman, James E.;
Kaptue Noche, L.

Publication type:

Article

Transferrin, Haptoglobin and Group-Specific Component Types in Tribal Populations of Andhra Pradesh.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 12, doi. 10.1159/000153081

By:

Goud, J.D.;
Rao, P.R.

Publication type:

Article

The '18' Variant of Human Placental Alkaline Phosphatase is Identical to the 'D-Variant'.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 18, doi. 10.1159/000153082

By:

Doellgast, George J.;
Kennedy, Martha;
Donald, Lynda J.

Publication type:

Article

Sjögren-Larsson Syndrome in Dizygous Twin Sisters.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 21, doi. 10.1159/000153083

By:

David, T.J.

Publication type:

Article

Human Red Cell Galactose-1-Phosphate Uridylyltransferase (EC 2.7.7.12).

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 27, doi. 10.1159/000153084

By:

Eriksen, Birthe;
Dissing, J.

Publication type:

Article

Genetic Studies of Red Cell Glutamic-Pyruvic Transaminase in Some Japanese Populations.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 33, doi. 10.1159/000153085

By:

Nishigaki, I.;
Itoh, T.;
Suzuki, H.;
Fujiki, N.

Publication type:

Article

Properdin Factor B Polymorphism in Afghanistan.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 39, doi. 10.1159/000153086

By:

Benkmann, H.G.;
Goedde, H.W.;
Agarwal, D.P.;
Flatz, G.;
Rahimi, A.;
Kaifie, S.;
Delbrück, H.

Publication type:

Article

Haptoglobin Types in Breast Carcinoma.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 44, doi. 10.1159/000153087

By:

Tsamantanis, C.;
Delinassios, J.G.;
Kottaridis, S.;
Christodoulou, C.

Publication type:

Article

C3 Polymorphism in Patients with Chronic Uremia.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 46, doi. 10.1159/000153088

By:

Stoffersen, Erik;
Jørgensen, Kaj Anker

Publication type:

Article

Hemoglobin New York Associated with Alpha-Thalassemia.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 50, doi. 10.1159/000153089

By:

Kendall, Alan;
Pang, Wing

Publication type:

Article

GPT Polymorphism in the Population of Bologna and Linkage Analysis with Beta-Thalassaemia.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 54, doi. 10.1159/000153090

By:

Facchini, F.;
Gruppioni, G.;
Veronesi-Martuzzi, F.;
Zannotti, M.

Publication type:

Article

A Further Report on a Kindred with Cases of 4p Trisomy and Monosomy.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 58, doi. 10.1159/000153091

By:

Mortimer, J.G.;
Chewings, W.E.;
Gardner, R.J.M.

Publication type:

Article

Association of Glyoxalase I Allotypes with Graves' Disease and Diabetes mellitus.

Published in:

Human Heredity, 1980, v. 30, n. 1, p. 62, doi. 10.1159/000153092

By:

Moens, Hilda;
Payne, Ronald;
Carter, Nicholas D.;
Farid, Nadir R.

Publication type:

Article