Works matching IS 00015652 AND DT 1988 AND VI 38 AND IP 4

Results: 11

Amelogenesis imperfecta:A Genetic Study.

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 189, doi. 10.1159/000153785

By:

Bäckman, B.;
Holmgren, G.

Publication type:

Article

Alpha-2-HS-Glycoprotein Polymorphism Detected in Human Urine by Isoelectric Focusing and Immunoblotting.

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 207, doi. 10.1159/000153786

By:

Kishi, K.;
Yasuda, T.;
Ikehara, Y.

Publication type:

Article

Alpha-Thalassemia in Northern Thailand.

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 211, doi. 10.1159/000153787

By:

Hundrieser, J.;
Sanguansermsri, T.;
Papp, T.;
Flatz, G.

Publication type:

Article

Family Studies of the E1kE1s Genotype for Plasma Cholinesterase.

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 228, doi. 10.1159/000153789

By:

Whittaker, Mary;
Britten, Judith J.;
Vyas, A.B.;
Hayes, T.C.

Publication type:

Article

Possible Influence of Major Gene Heterozygosity on Variation of Quantitative Traits.

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 216, doi. 10.1159/000153788

By:

Bishop, G.R.;
Mayo, O.;
Beckman, L.

Publication type:

Article

DNA Haplotypes and Frameworks Associated with the Beta-Globin Gene in the Kachari Population of Assam (India).

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 240, doi. 10.1159/000153791

By:

Hundrieser, J.;
Deka, R.;
Gogoi, B.C.;
Papp, T.;
Flatz, G.

Publication type:

Article

Recognition of Two New Phenotypes Segregating the E1k Allele for Plasma Cholinesterase.

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 233, doi. 10.1159/000153790

By:

Whittaker, Mary;
Britten, Judith J.

Publication type:

Article

Three Japanese Families with Members Carrying C7 Silent Allele (C7*Q0).

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 246, doi. 10.1159/000153792

By:

Nishimukai, Hiroaki;
Kitamura, Hajime;
Takeuchi, Yoshihiro;
Shinomiya, Takaaki;
Tamaki, Yoshihiro

Publication type:

Article

Interaction between ABO and Haptoglobin in a White Australian Population.

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 251, doi. 10.1159/000153793

By:

Mitchell, R.J.;
Eslick, C.J.

Publication type:

Article

Formal Genetics of Esterase D (EC 3.1.1.1): Evidence for a Sex-Phenotype Association.

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 255, doi. 10.1159/000153794

By:

Amorim, António;
Rocha, Jorge;
Kömpf, Jost;
Ritter, Horst

Publication type:

Article

Distribution of Transferrin Subtypes in Aragon (North-East Spain).

Published in:

Human Heredity, 1988, v. 38, n. 4, p. 258, doi. 10.1159/000153795

By:

Martinez-Janeta, B.;
Castellano, M.

Publication type:

Article

Works matching IS 00015652 AND DT 1988 AND VI 38 AND IP 4

Amelogenesis imperfecta:A Genetic Study.

Alpha-2-HS-Glycoprotein Polymorphism Detected in Human Urine by Isoelectric Focusing and Immunoblotting.

Alpha-Thalassemia in Northern Thailand.

Family Studies of the E<sub>1</sub><sup>k</sup>E<sub>1</sub><sup>s</sup> Genotype for Plasma Cholinesterase.

Possible Influence of Major Gene Heterozygosity on Variation of Quantitative Traits.

DNA Haplotypes and Frameworks Associated with the Beta-Globin Gene in the Kachari Population of Assam (India).

Recognition of Two New Phenotypes Segregating the E<sub>1</sub><sup>k</sup> Allele for Plasma Cholinesterase.

Three Japanese Families with Members Carrying C7 Silent Allele (C7*Q0).

Interaction between ABO and Haptoglobin in a White Australian Population.

Formal Genetics of Esterase D (EC 3.1.1.1): Evidence for a Sex-Phenotype Association.

Distribution of Transferrin Subtypes in Aragon (North-East Spain).