Works matching IS 00015652 AND DT 1993 AND VI 43 AND IP 3

Results: 11

Chromosomal Anomalies in 1,000 Children Referred with Suspected Genetic Disorders.

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 137, doi. 10.1159/000154168

By:

Navsaria, Dipesh;
Mathews, Thomas;
Conte, Robert A.;
Verma, Ram S.

Publication type:

Article

Genetic Structure in the Garfagnana (Tuscany, Italy): A Study of Eight Protein Markers by Isoelectric Focusing.

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 186, doi. 10.1159/000154175

By:

Weidinger, Sebastian;
Hallwachs, Roland;
Paoli, Giorgio;
Stanyon, Roscoe

Publication type:

Article

Isonymy in Haemoglobinopathies in a Sicilian Sample.

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 203, doi. 10.1159/000154178

By:

Schiliró, G.;
Rodríguez-Larralde, A.;
Mamolini, E.;
Scapoli, C.;
Barrai, I.

Publication type:

Article

Complex Segregation Analysis of Thyroid Autoantibodies: Are They Inherited as an Autosomal Dominant Trait?

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 141, doi. 10.1159/000154169

By:

Phillips, D.I.W;
Shields, D.C.;
Dugoujon, J.M.;
Prentice, L.;
McGuffin, P.;
Smith, Rees

Publication type:

Article

Population Studies in Northern Sweden 18. Geographical Covariation between Hypercholesterolemia and Finnish Genetic Influence.

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 147, doi. 10.1159/000154170

By:

Nylander, P.-O.;
Asplund, K.;
Beckman, L.;
Stegmayr, B.;
Johansson, I.

Publication type:

Article

A Point Mutation in the Cl-inhibitor Gene Causes Type I Hereditary Angiooedema.

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 155, doi. 10.1159/000154171

By:

Siddique, Z.;
McPhaden, A.R.;
Fothergill, J.E.;
Whaley, K.

Publication type:

Article

Direct Phenotyping of Human Apolipoprotein E in Plasma: Application to Population Frequency Distribution in Paris (France).

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 159, doi. 10.1159/000154172

By:

Bailleul, S.;
Couderc, R.;
Landais, V.;
Lefèvre, G.;
Raichvarg, D.;
Etienne, J.

Publication type:

Article

Methodological Issues in Linkage Analyses for Psychiatric Disorders: Secular Trends, Assortative Mating, Bilineal Pedigrees.

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 166, doi. 10.1159/000154173

By:

Spence, Anne;
Bishop, Timothy;
Boehnke, Michael;
Elston, Robert C.;
Falk, Catherine;
Hodge, Susan E.;
Ott, Jürg;
Rice, John;
Merikangas, Kathleen;
Kupfer, David

Publication type:

Article

A Procedure for Combining Two-Point Lod Scores into a Summary Multipoint Map.

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 173, doi. 10.1159/000154174

By:

Curtis, David;
Gurling, Hugh

Publication type:

Article

Molecular Characterization of 21-Hydroxylase Deficiency in 70 Italian Families.

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 190, doi. 10.1159/000154176

By:

Carrera, P.;
Ferrari, M.;
Beccaro, F.;
Spiga, I.;
Zanussi, M.;
Rigon, F.;
Braggion, F.;
Zacchello, F.;
Greggio, N.

Publication type:

Article

Microsatellite Polymorphisms for Chromosome 5 Bands q11.2-q13.3.

Published in:

Human Heredity, 1993, v. 43, n. 3, p. 197, doi. 10.1159/000154177

By:

Sherrington, Robin;
Mankoo, Baljinder;
Dixon, Mike;
Curtis, David;
Kalsi, Gursharon;
Melmer, Georg;
Gurling, Hugh

Publication type:

Article