Works matching IS 00015652 AND DT 1995 AND VI 45 AND IP 1

Results: 10

Linkage Analysis between Schizophrenia and Index Simple-Sequence Repeat Loci for Chromosome 21.

Published in:

Human Heredity, 1995, v. 45, n. 1, p. 49, doi. 10.1159/000154254

By:

Byerley, William;
Hoff, Mark;
Holik, John;
Myles-Worsley, M.;
Waldo, M.;
Freedman, R.;
Coon, Hilary

Publication type:

Article

Placental Alkaline Phosphatase Types and Transplacental IgG Transport.

Published in:

Human Heredity, 1995, v. 45, n. 1, p. 1, doi. 10.1159/000154247

By:

Beckman, G.;
Beckman, L.;
Holm, S.;
Silkström, C.;
Wennberg, C.

Publication type:

Article

The Affected-Pedigree-Member Method: Power to Detect Linkage.

Published in:

Human Heredity, 1995, v. 45, n. 1, p. 13, doi. 10.1159/000154250

By:

Weeks, Daniel E.;
Harby, Lisa D.

Publication type:

Article

An X-Linked Version of the Affected-Pedigree-Member Method of Linkage Analysis.

Published in:

Human Heredity, 1995, v. 45, n. 1, p. 25, doi. 10.1159/000154251

By:

Weeks, Daniel E.;
Valappil, Thamban I.;
Schroeder, Mark;
Brown, Deborah L.

Publication type:

Article

Chinese Population Data on the PCR-Based Loci HLA-DQ Alpha, Low-Density-Lipoprotein Receptor, Glycophorin A, Hemoglobin γ<sup>G</sup>, D7S8, and Group-Specific Component.

Published in:

Human Heredity, 1995, v. 45, n. 1, p. 34, doi. 10.1159/000154252

By:

Huang, Nu En;
Budowle, Bruce

Publication type:

Article

Segregation Analysis of Colorectal Cancer in Northern Ireland.

Published in:

Human Heredity, 1995, v. 45, n. 1, p. 41, doi. 10.1159/000154253

By:

Houlston, R.S.;
Collins, A.;
Kee, F.;
Collins, B.J.;
Shields, D.C.;
Morton, N.E.

Publication type:

Article

Identical Intragenic Microsatellite Haplotype Found in Cystic Fibrosis Chromosomes Bearing Mutation G551D in Irish, English, Scottish, Breton and Czech Patients.

Published in:

Human Heredity, 1995, v. 45, n. 1, p. 6, doi. 10.1159/000154249

By:

Cashman, S.M.;
Patino, A.;
Martinez, A.;
Garcia-Delgado, M.;
Miedzybrodzka, Z.;
Schwarz, M.;
Shrimpton, A.;
Ferec, C.;
Raguenes, O.;
Macek, Jr., M.;
Morral, N.;
De Arce, M.

Publication type:

Article

Identification of a Novel Missense Mutation G239R in Exon 6a of the CFTR Gene.

Published in:

Human Heredity, 1995, v. 45, n. 1, p. 53, doi. 10.1159/000154255

By:

Bienvenu, Thierry;
Cazeneuve, Cecile;
Fajac, Isabelle;
Dusser, Daniel;
Hubert, Dominique;
Kaplan, Jean Claude;
Beldjord, Cherif

Publication type:

Article

Frequency of Delta-F508 Mutation and XV2C/KM19 Haplotypes in Cuban Cystic Fibrosis Families.

Published in:

Human Heredity, 1995, v. 45, n. 1, p. 55, doi. 10.1159/000154256

By:

Collazo, T.;
Magarino, C.;
Chavez, R.;
Suardiaz, B.;
Gispert, S.;
Gomez, M.;
Rojo, M.;
Heredero, L.

Publication type:

Article

Joint Phenotype Distribution at the Esterase D and Complement C3 Loci in the Upper Silesia Population (Poland).

Published in:

Human Heredity, 1995, v. 45, n. 1, p. 58, doi. 10.1159/000154257

By:

Raczek, Ewa;
Kabiesz, Jadwiga

Publication type:

Article