Works matching IS 00015652 AND DT 1992 AND VI 42 AND IP 3

Results: 15

BF and C3 Genetic Polymorphisms in Kaingang Indians from Southern Brazil.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 153, doi. 10.1159/000154058

By:

Guerra, Leila Karazawa;
Rehfeldt, Ian Robert;
Lima, Marcilene Teixeira;
Petzl-Erler, Maria Luiza;
de Messias, Iara J. Taborda

Publication type:

Article

Hereditary Nonspherocytic Hemolytic Anemia Due to Pyruvate Kinase Deficiency: A Prevalence Study in Quebec (Canada).

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 179, doi. 10.1159/000154063

By:

de Medicis, Eveline;
Ross, Peter;
Friedman, Ronald;
Hume, Heather;
Marceau, Danielle;
Milot, Marcel;
Lyonnais, Jean;
de Braekeleer, Marc

Publication type:

Article

Uniparental Origin of Sex Chromosome Polysomies.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 193, doi. 10.1159/000154066

By:

Lorda-Sanchez, Isabel;
Binkert, Franz;
Hinkel, Klaus Georg;
Moser, Hans;
Rosenkranz, Walter;
Maechler, Marco;
Schinzel, Albert

Publication type:

Article

A Polymorphic Complex Dinucleotide Repeat at the Telomeric D8S7 Locus.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 149, doi. 10.1159/000154057

By:

Wood, Stephen;
Schertzer, Michael

Publication type:

Article

Announcement.

Published in:: Human Heredity, 1992, v. 42, n. 3, p. 208, doi. 10.1159/000154071
Publication type:: Article

Limited Genetic Diversity in Polynesians Reflected in the Highly Polymorphic 3'HVRα-Globin Gene Marker.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 157, doi. 10.1159/000154059

By:

Hertzberg, M.S.;
Mickleson, K.N.P.;
Trent, R.J.

Publication type:

Article

Complement Genetic Markers in Schizophrenia: C3, BF and C6 Polymorphisms.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 162, doi. 10.1159/000154060

By:

Fañanás, L.;
Moral, P.;
Panadero, M.A.;
Bertranpetit, J.

Publication type:

Article

Serum Protein Groups (Hp, GC, C3) in Patients with Gastric Carcinoma.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 168, doi. 10.1159/000154061

By:

Theodoropoulos, G.;
Archimandritis, A.;
Germenis, A.;
Malamas, N.;
Tjivras, M.;
Fertakis, A.

Publication type:

Article

Complementation in Zellweger Syndrome: Biochemical Analysis of Newly Generated Peroxisomes.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 172, doi. 10.1159/000154062

By:

Stanczak, H.;
Kremser, K.;
Singh, A.K.;
Ashcraft, J.;
Stanley, W.;
Singh, I.

Publication type:

Article

The First Case of Familial Amyloidotic Polyneuropathy (FAP Met30) in the Finnish Population.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 184, doi. 10.1159/000154064

By:

Drugge, Ulf;
Holmgren, Gösta;
Udd, Bjarne

Publication type:

Article

A Rapid Method for Diagnosis of the Lebanese Allele in the Low-Density Lipoprotein Receptor Gene.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 189, doi. 10.1159/000154065

By:

Cavanaugh, J.A.;
Easteal, S.;
Simons, L.;
Serjeantson, S.

Publication type:

Article

GC and C3 Serum Groups in Peptic Ulcer.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 198, doi. 10.1159/000154067

By:

Archimandritis, A.;
Douvara, M.;
Grigoris, S.;
Tjivras, M.;
Davaris, P.;
Fertakis, A.

Publication type:

Article

Interaction between ABO and Haptoglobin Systems in a Bengalee Population.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 201, doi. 10.1159/000154068

By:

Bandopadhaya, Arup Ratan

Publication type:

Article

Haplotype Analysis and Polymorphic Frequency Data at Two Factor IX Loci (F9-192 and F9-Hha1) in a Chinese Population.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 204, doi. 10.1159/000154069

By:

Chen, S.H.;
Wang, N.S.;
Schoof, J.;
Scott, C.R.

Publication type:

Article

PI*E Tripoli: A New Allele in the Alpha-1-Antitrypsin System.

Published in:

Human Heredity, 1992, v. 42, n. 3, p. 206, doi. 10.1159/000154070

By:

Sebetan, Ismail M.

Publication type:

Article