Works matching IS 00015652 AND DT 1997 AND VI 47 AND IP 5

Results: 10

Ethnic Differences in the HFE Codon 282 (Cys/Tyr) Polymorphism.

Published in:

Human Heredity, 1997, v. 47, n. 5, p. 263, doi. 10.1159/000154422

By:

Beckman, L.E.;
Saha, N.;
Spitsyn, V.;
Van Landeghem, G.;
Beckman, L.

Publication type:

Article

Investigation of Complement C4B Deficiency in Schizophrenia.

Published in:

Human Heredity, 1997, v. 47, n. 5, p. 279, doi. 10.1159/000154424

By:

Schroers, Roland;
Nöthen, Markus M.;
Rietschel, Marcella;
Albus, Margot;
Maier, Wolfgang;
Schwab, Sybille;
Wildenauer, Dieter;
Fimmers, Rolf;
Propping, Peter;
Dewald, Georg

Publication type:

Article

Paternity Analysis in Cases of Father-Daughter Incest Using Multiallelic Loci.

Published in:

Human Heredity, 1997, v. 47, n. 5, p. 288, doi. 10.1159/000154426

By:

Cifuentes O., Lucía;
Jorquera G., Hugo

Publication type:

Article

The Spectrum of Beta-Thalassaemia Mutations in the Lebanon.

Published in:

Human Heredity, 1997, v. 47, n. 5, p. 241, doi. 10.1159/000154419

By:

Zahed, L.;
Talhouk, R.;
Saleh, M.;
Abou-Jaoudeh, R.;
Fisher, C.;
Old, J.

Publication type:

Article

Angiotensin-Converting Enzyme Deletion Polymorphism Is Associated with Hypertension in a Sikh Population.

Published in:

Human Heredity, 1997, v. 47, n. 5, p. 250, doi. 10.1159/000154420

By:

Mastana, Sarabjit;
Nunn, Janice

Publication type:

Article

Molecular and Cytogenetic Investigations of the Fragile X Region Including the Frax A and Frax E CGG Trinucleotide Repeat Sequences in Families Multiplex for Autism and Related Phenotypes.

Published in:

Human Heredity, 1997, v. 47, n. 5, p. 254, doi. 10.1159/000154421

By:

Gurling, H.M.D.;
Bolton, P.F.;
Vincent, J.;
Melmer, G.;
Rutter, M.

Publication type:

Article

Linkage Analysis of Manic Depression (Bipolar Affective Disorder) in Icelandic and British Kindreds using Markers on the Short Arm of Chromosome 18.

Published in:

Human Heredity, 1997, v. 47, n. 5, p. 268, doi. 10.1159/000154423

By:

Kalsi, G.;
Smyth, C.;
Brynjolfsson, J.;
Sherrington, R.S.;
O'Neill, J.;
Curtis, D.;
Rifkin, L.;
Murphy, P.;
Petursson, H.;
Gurling, H.M.D.

Publication type:

Article

Haptoglobin Polymorphism in Korean Patients with Cardiovascular Diseases.

Published in:

Human Heredity, 1997, v. 47, n. 5, p. 283, doi. 10.1159/000154425

By:

Hong, Seung Ho;
Kang, Byung Yong;
Lim, Jeom Hee;
Namkoong, Yong;
Oh, Moon You;
Kim, Jin Q.;
Lee, Chung Choo

Publication type:

Article

A CA Repeat in the First Intron of the CFTR Gene.

Published in:

Human Heredity, 1997, v. 47, n. 5, p. 295, doi. 10.1159/000154427

By:

Moulin, Danielle S.;
Smith, Annabel N.;
Harris, Ann

Publication type:

Article

Association between Allele 1 of T102C Polymorphism, 5-Hydroxytryptamine 2a Receptor Gene and Schizophrenia in Chinese Males in Singapore.

Published in:

Human Heredity, 1997, v. 47, n. 5, p. 298, doi. 10.1159/000154428

By:

Tay, A.H.N.;
Lim, L.C.C.;
Lee, W.L.;
Wong, K.E.;
Wong, L.Y.;
Tsoi, W.F.

Publication type:

Article