Works matching IS 00015652 AND DT 1980 AND VI 30 AND IP 4

Results: 15

Is the HpO Phenomenon in Tropical Populations Really Genetic?

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 201, doi. 10.1159/000153127

By:

Rougemont, A.;
Quilici, M.;
Delmont, J.;
Ardissone, J.P.

Publication type:

Article

Some Biochemical Polymorphisms in Members of the Gaddi Tribe of Himachal Pradesh.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 204, doi. 10.1159/000153128

By:

Kaur, Harsurinder;
Sehajpal, P.K.;
Khanna, A.K.;
Shrivastava, P.K.

Publication type:

Article

Isoenzymes of Red Cell Glyoxalase I (EC 4.4.1.5) in a Finnish Population.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 207, doi. 10.1159/000153129

By:

Uotila, Lasse;
Koivusalo, Martti

Publication type:

Article

Polymorphism of the Sixth Component of Complement (C6) in Norwegian Lapps.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 211, doi. 10.1159/000153130

By:

Olvíng, J.H.;
Teisberg, P.;
Olaisen, B.

Publication type:

Article

Search for Linkage between Dermatoglyphic Sole Characters and Blood Groups.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 215, doi. 10.1159/000153131

By:

Bener, Abdülbari

Publication type:

Article

Plasma Protein and Enzyme Polymorphisms in Belgium.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 221, doi. 10.1159/000153132

By:

Brocteur, J.;
Hoste, B.;
André, A.

Publication type:

Article

Mohr-Wriedt (A<sub>2</sub>) Brachydactyly.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 225, doi. 10.1159/000153133

By:

Freire-Maia, N.;
Maia, Néria A.;
Pacheco, C.N.A.

Publication type:

Article

Erythrocyte Glyoxalase I and Esterase D Polymorphisms in Four French Populations.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 232, doi. 10.1159/000153134

By:

Vergnes, H.;
Meyer, S.;
Weil, D.;
Goudemand, J.;
Brevière, D.;
Sevin, J.;
Constans, J.

Publication type:

Article

Frequencies of Gm and Km Allotypes in the Population of Singapore, Sri Lanka and Punjabis in North India.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 237, doi. 10.1159/000153135

By:

Daveau, Maryvonne;
Rivat, Liliane;
Lalouel, J.M.;
Langaney, A.;
Roberts, D.F.;
Simons, M.J.

Publication type:

Article

Polymorphism of the Second Component of Complement (C2) in Graves' Disease.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 245, doi. 10.1159/000153136

By:

Noel, Elke P.;
Sampson, Laura;
Pepper, Barbara M.;
Farid, Nadir R.

Publication type:

Article

Electrophoretic Investigation of y-Glutamyl-Cyclotransferase from Human Erythrocytes.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 248, doi. 10.1159/000153137

By:

Board, P.G.

Publication type:

Article

Population Studies in Cameroon.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 251, doi. 10.1159/000153138

By:

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

Publication type:

Article

Glyoxalase I (GLO; EC 4.4.1.5).

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 259, doi. 10.1159/000153139

By:

Al-Agidi, Saad K.;
Papiha, Surinder S.;
Shukri, Suham M.

Publication type:

Article

High Frequency of In<sup>a</sup> Antigen Among Iranians and Arabs.

Published in:

Human Heredity, 1980, v. 30, n. 4, p. 262, doi. 10.1159/000153140

By:

Badakere, S.S.;
Vasantha, K.;
Bhatia, H.M.;
Ala, F.;
Clarke, V.A.;
Moesri, Rustom;
Sommai, Sringarm;
Amin, A.B.

Publication type:

Article

Book Review.

Published in:: Human Heredity, 1980, v. 30, n. 4, p. 264, doi. 10.1159/000153141
Publication type:: Article