Works matching IS 00015652 AND DT 1998 AND VI 48 AND IP 4

Results: 10

Transferrin Variants as Markers of Migrations and Admixture between Populations in the Baltic Sea Region.

Published in:

Human Heredity, 1998, v. 48, n. 4, p. 185, doi. 10.1159/000022800

By:

Beckman, L.;
Sikström, C.;
Mikelsaar, A.-V.;
Krumina, A.;
Ambrasiene, D.;
Kučinskas, V.;
Beckman, G.

Publication type:

Article

Glucose-6-Phosphate Dehydrogenase Deficiency and Homozygous Sickle Cell Disease in Congo.

Published in:

Human Heredity, 1998, v. 48, n. 4, p. 192, doi. 10.1159/000022801

By:

Bouanga, Jean Claude;
Mouélé, René;
Préhu, Claude;
Wajcman, Henri;
Feingold, Josué;
Galactéros, Frédéric

Publication type:

Article

Familial Psoriasis and HLA-B: Unambiguous Support for Linkage in 97 Published Families.

Published in:

Human Heredity, 1998, v. 48, n. 4, p. 198, doi. 10.1159/000022802

By:

Leder, Richard O.;
Mansbridge, Jonathan N.;
Hallmayer, Joachim;
Hodge, Susan E.

Publication type:

Article

Negative Association between T102C Polymorphism of the 5-HT<sub>2a</sub> Receptor Gene and Schizophrenia in Japan.

Published in:

Human Heredity, 1998, v. 48, n. 4, p. 212, doi. 10.1159/000022803

By:

Shinkai, Takahiro;
Ohmori, Osamu;
Kojima, Hideki;
Terao, Takeshi;
Suzuki, Takashi;
Abe, Kazuhiko

Publication type:

Article

High Variability of CYP21 Gene Rearrangements in Spanish Patients with Classic Form of Congenital Adrenal Hyperplasia.

Published in:

Human Heredity, 1998, v. 48, n. 4, p. 216, doi. 10.1159/000022804

By:

Lobato, M. Natividad;
Aledo, Rosa;
Meseguer, Anna

Publication type:

Article

A Novel MspI PCR-RFLP in the Human Cytosine 5-Methyltransferase Gene: Lack of Relevance for Malignant Lymphoproliferative Disease and Breast Cancer.

Published in:

Human Heredity, 1998, v. 48, n. 4, p. 226, doi. 10.1159/000022805

By:

Bagwe, Aparna N.;
Ahmed, Mohammed O.;
Franchina, M.;
Spagnolo, Dominic V.;
Papadimitriou, John M.;
Kay, Peter H.

Publication type:

Article

Molecular Variants of Luteinizing Hormone in Three Populations of Southeast Asia.

Published in:

Human Heredity, 1998, v. 48, n. 4, p. 232, doi. 10.1159/000022807

By:

Ramanujam, Lakshmi;
Liao, Wu-Xiang;
Roy, Ashim C.;
Ng, Soon Chye;
Ratnam, Shan S.

Publication type:

Article

HpaII Polymerase Chain Reaction Restriction Fragment Length Polymorphism in the Human CD19 Gene on 16p11.

Published in:

Human Heredity, 1998, v. 48, n. 4, p. 230, doi. 10.1159/000022806

By:

Thunberg, U.;
Gidlöf, C.;
Bånghagen, M.;
Sällström, J.F.;
Sundström, C.;
Tötterman, T.

Publication type:

Article

Exclusion of Identified LGMD1 Loci from Four Dominant Limb-Girdle Muscular Dystrophy Families.

Published in:

Human Heredity, 1998, v. 48, n. 4, p. 179, doi. 10.1159/000022799

By:

Speer, Marcy C.;
Vance, Jeffery M.;
Lennon-Graham, Felicia;
Stajich, Jeffrey M.;
Viles, Kristi D.;
Gilchrist, James M.;
Nigro, Vincenzo;
McMichael, Robert;
Chutkow, Jerry G.;
Bartoloni, Lucia;
Horrigan, Steven K.;
Westbrook, Carol A.;
Pericak-Vance, Margaret A.

Publication type:

Article

CA Repeat Polymorphism of theCOL6A3 Gene on Chromosome 2 q37.

Published in:

Human Heredity, 1998, v. 48, n. 4, p. 235, doi. 10.1159/000022808

By:

Pan, Te-Cheng;
Zhang, Rui-Zhu;
Speer, Marcy C.;
Chu, Mon-Li

Publication type:

Article