Works matching IS 00015652 AND DT 1991 AND VI 41 AND IP 3

Results: 11

Transferrin Types in Different Ethnic Groups of the USSR and Mongolia.

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 201, doi. 10.1159/000154001

By:

Titenko, N.V.;
Spitsyn, V.A.;
Alekseeva, T.I.

Publication type:

Article

DNA Polymorphism and Linkage Disequilibrium within the Apolipoprotein CII Locus on Human Chromosome 19.

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 188, doi. 10.1159/000153999

By:

MacKenzie, Alex E.;
MacLeod, Heather L.;
Leblond, Suzanne C.;
Monteith, Nancy;
Lahey, Donelda;
Korneluk, Robert G.

Publication type:

Article

Forensic Applications of Molecular Genetic Analysis: An Italian Collaborative Study on Paternity Testing by the Determination of Variable Number of Tandem Repeat DNA Polymorphisms.

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 174, doi. 10.1159/000153997

By:

Gasparini, P.;
Mandich, P.;
Novelli, G.;
Bellone, E.;
Sangiuolo, F.;
De Stefano, F.;
Potenza, L.;
Trabetti, E.;
Marigo, M.;
Pignatti, P.F.;
Dallapiccola, B.;
Ajmar, F.

Publication type:

Article

Hereditary Disorders in Saguenay-Lac-St-Jean (Quebec, Canada).

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 141, doi. 10.1159/000153992

By:

De Braekeleer, Marc

Publication type:

Article

Association between the Acid Phosphatase 1 and Adenosine Deaminase Systems in a Brazilian Sample.

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 147, doi. 10.1159/000153993

By:

Engrácia, V.;
Mestriner, M.A;
Cabello, P.H.;
Krieger, H.

Publication type:

Article

Impact of Heredity in Myopia.

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 151, doi. 10.1159/000153994

By:

Teikari, J.M.;
O'Donnell, J.;
Kaprio, J.;
Koskenvuo, M.

Publication type:

Article

Population Studies in Northern Sweden.

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 157, doi. 10.1159/000153995

By:

Nylander, P.-O.;
Beckman, L.

Publication type:

Article

Founder Effect in Familial Hyperchylomicronemia among French Canadians of Quebec.

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 168, doi. 10.1159/000153996

By:

De Braekeleer, Marc;
Dionne, Carole;
Gagné, Claude;
Julien, Pierre;
Brun, Daniel;
Ven Murthy, M.R.;
Paul-J.Lupien, P.

Publication type:

Article

Protease Inhibitor Frequencies: Is There a Deficit of M Subtype Heterozygotes?

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 182, doi. 10.1159/000153998

By:

Whitfield, J.B.

Publication type:

Article

Polymorphism of Complement Component I in Mongoloid Populations: A New Genetic Variant IF A2.

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 206, doi. 10.1159/000154002

By:

Ding, Mei;
Umetsu, Kazuo;
Yuasa, Isao;
Nakamura, Shigeki;
Choi, Won Young;
Suzuki, Tsuneo

Publication type:

Article

Segregation Distortions of the ABO and Rh Systems in Malformed Newborns.

Published in:

Human Heredity, 1991, v. 41, n. 3, p. 195, doi. 10.1159/000154000

By:

Cifuentes, Lucia;
Nazer, Julio;
Valenzuela, Carlos Y.

Publication type:

Article