Works matching IS 00015652 AND DT 1996 AND VI 46 AND IP 3

Results: 11

Butyrylcholinesterase Variants (BCHE and CHE2 Loci) Associated with Erythrocyte Acetylcholinesterase Inhibition in Farmers Exposed to Pesticides.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 142, doi. 10.1159/000154343

By:

Fontoura-da-Silva, S.E.;
Chautard-Freire-Maia, E.A.

Publication type:

Article

Detection of Four Novel Mutations in the Porphobilinogen Deaminase Gene in French Caucasian Patients with Acute Intermittent Porphyria.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 177, doi. 10.1159/000154349

By:

Puy, H.;
Deybach, J.C.;
Lamoril, J.;
Robreau, A.M.;
Nordmann, Y.

Publication type:

Article

The Codon 31 Polymorphism of the p53-lnducible Gene p21 Shows Distinct Differences between Major Ethnic Groups.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 148, doi. 10.1159/000154344

By:

Birgander, R.;
Själander, A.;
Saha, N.;
Spitsyn, V.;
Beckman, L.;
Beckman, G.

Publication type:

Article

Distribution of Composite CYP1A1 Genotypes in Africans, African-Americans and Caucasians.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 121, doi. 10.1159/000154339

By:

Garte, Seymour J.;
Trackman, Julie;
Crofts, Frances;
Toniolo, Paolo;
Buxbaum, Joel;
Bayo, Sine;
Taioli, Emanuela

Publication type:

Article

Phenylketonuria in Costa Rica: Preliminary Spectrum of PAH Mutations and Their Associations with Highly Polymorphic Haplotypes.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 128, doi. 10.1159/000154340

By:

Santos, María;
Kuzmin, Alexei I.;
Eisensmith, Randy C.;
Goltsov, Alexei A.;
Woo, Savio L.C.;
Barrantes, Ramiro;
de Céspedes, Carlos

Publication type:

Article

Molecular Characterization of Erythrocyte Glucose-6-Phosphate Dehydrogenase Deficiency in Al-Ain District, United Arab Emirates.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 136, doi. 10.1159/000154342

By:

Bayoumi, R.A.;
Nur-E-Kamal, M.S.A.;
Tadayyon, M.;
Mohamed, K.K.A.;
Mahboob, B.H.;
Qureshi, M.M.;
Lakhani, M.S.;
Awaad, M.O.;
Kaeda, J.;
Vulliamy, T.J.;
Luzzatto, L.

Publication type:

Article

Coagulation Factor XIIIA Subtypes in Brazilian Indians.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 132, doi. 10.1159/000154341

By:

Arnold, G.;
Kömpf, J.;
Salzano, F.M.

Publication type:

Article

A Splicing Mutation in Intron 16 of the Cystic Fibrosis Transmembrane Conductance Regulator Gene, Associated with Severe Disease, Is Common on Reunion Island.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 168, doi. 10.1159/000154347

By:

Bienvenu, T.;
Cartault, F.;
Lesure, F.;
Renouil, M.;
Beldjord, C.;
Kaplan, J.C.

Publication type:

Article

Sharing at the Major Histocompatibility Complex Affects the Secondary Sex Ratio in Differing Ways.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 155, doi. 10.1159/000154345

By:

Astolfi, Paola;
Cuccia, Mariaclara;
Caruso, Calogero;
Favoino, Biagio;
Fazzari, Marianna;
Mantovani, Vilma;
Lulli, Patrizia;
Illeni, Maria Teresa;
Martinetti, Miryam

Publication type:

Article

2176insC: A Novel Mutation in Exon 13 of the Cystic Fibrosis Gene.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 166, doi. 10.1159/000154346

By:

Savov, Alexey;
Angelicheva, Dora;
Jordanova, Albena;
Kremensky, Ivo;
Kalaydjieva, Luba

Publication type:

Article

Molecular Characterization of G6PD Deficiency in Oman.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 172, doi. 10.1159/000154348

By:

Daar, Shahina;
Vulliamy, Tom J.;
Kaeda, Jaspal;
Mason, Philip J.;
Luzzatto, Lucio

Publication type:

Article