Works matching IS 00015652 AND DT 1999 AND VI 49 AND IP 1

Results: 15

Analysis of Three Suggested Psoriasis Susceptibility Loci in a Large Swedish Set of Families: Confirmation of Linkage to Chromosome 6p (HLA Region), and to 17q, but not to 4q.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 2, doi. 10.1159/000022832

By:

Enlund, Fredrik;
Samuelsson, Lena;
Enerbäck, Charlotta;
Inerot, Annica;
Wahlström, Jan;
Yhr, Maria;
Torinsson, Åsa;
Martinsson, Tommy;
Swanbeck, Gunnar

Publication type:

Article

Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 9, doi. 10.1159/000022833

By:

Bachega, Tânia A.S.S.;
Billerbeck, Ana Elisa C.;
Madureira, Guiomar;
Arnhold, Ivo J.P.;
Medeiros, Maria A.;
Marcondes, José A.M.;
Longui, Carlos A.;
Nicolau, Willian;
Bloise, Walter;
Mendonca, Berenice B.

Publication type:

Article

Allele Frequencies in a Worldwide Survey of a CA Repeat in the First Intron of the CFTR Gene.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 15, doi. 10.1159/000022834

By:

Mateu, Eva;
Calafell, Francesc;
Bonné-Tamir, Batsheva;
Kidd, Judith R.;
Casals, Teresa;
Kidd, Kenneth K.;
Bertranpetit, Jaume

Publication type:

Article

Polymorphisms in the HFE Gene.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 21, doi. 10.1159/000022835

By:

Douabin, Véronique;
Moirand, Romain;
Jouanolle, Anne-Marie;
Brissot, Pierre;
Le Gall, Jean-Yves;
Deugnier, Yves;
David, Véronique

Publication type:

Article

Determination of the Allele Frequencies of Three Polymorphisms in the Promoter Region of the Human Protein C Gene in Three Brazilian Ethnic Groups.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 27, doi. 10.1159/000022836

By:

Mendes, Christiane P.O.;
Hackel, Christine;
Arruda, Valder R.;
Annichino-Bizzacchi, Joyce M.

Publication type:

Article

Apolipoprotein B 5'-Ins/Del and 3'-VNTR Polymorphisms in Chinese, Malay and Indian Singaporeans.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 31, doi. 10.1159/000022837

By:

Choong, M.L.;
Koay, E.S.C.;
Khaw, M.C.;
Aw, T.C.

Publication type:

Article

Population Study of Common Glucose-6-Phosphate Dehydrogenase Mutations in Kuwait.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 41, doi. 10.1159/000022838

By:

Samilchuk, Elena;
D'Souza, Brendan;
Al-Awadi, Sadika

Publication type:

Article

Variable Distribution of TFF2 (Spasmolysin) Alleles in Europeans Does Not Indicate Predisposition to Gastric Cancer.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 45, doi. 10.1159/000022839

By:

dos Santos Silva, Elisabeth;
Kayademir, Tuncay;
Regateiro, Fernando;
Machado, José Carlos;
Savas, Sevtap;
Dobosz, Tadeusz;
Blin, Nikolaus;
Gött, Peter

Publication type:

Article

Genomic Distribution and Gonadal mRNA Expression of Two Human Luteinizing Hormone Receptor Exon 1 Sequences in Random Populations.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 48, doi. 10.1159/000022840

By:

Tsai-Morris, Chon Hwa;
Geng, Yi;
Buczko, Ellen;
Dehejia, Anindya;
Dufau, Maria L.

Publication type:

Article

α<sub>1</sub>-Antitrypsin (PI) Alleles as Markers of Westeuropean Influence in the Baltic Sea Region.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 52, doi. 10.1159/000022841

By:

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

Publication type:

Article

Identification in Portugal and Brazil of a mtDNA Lineage Containing a 9-bp Triplication of the Intergenic COII/tRNA<sup>Lys</sup> Region.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 56, doi. 10.1159/000022842

By:

Alves-Silva, Juliana;
Guimarães, Pedro E.M.;
Rocha, Jorge;
Pena, Sérgio D.J.;
Prado, Vania F.

Publication type:

Article

A Novel Mutation (R271X) in the Myotubularin Gene Causes a Severe Miotubular Myopathy.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 59, doi. 10.1159/000022843

By:

De Luca, Alessandro;
Torrente, Isabella;
Mangino, Massimo;
Bertini, Enrico;
Dallapiccola, Bruno;
Novelli, Giuseppe

Publication type:

Article

Allele Frequency of D17S855 Microsatellite Locus in Japanese People.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 61, doi. 10.1159/000022844

By:

Yokozaki, Hiroshi;
Tahara, Eiichi

Publication type:

Article

Absence of the Derived Allele at the DYS199 Locus in 3 NE Chinese Populations.

Published in:

Human Heredity, 1999, v. 49, n. 1, p. 63, doi. 10.1159/000022845

By:

Wang, Bai-qiu;
Fu, Song-bin;
Sun, Yan-Yang;
Huang, Cheng-bin;
Yang, Huan-jie;
Xue, Ya-li;
Wang, Qi;
Zhang, Gui-yin;
Li, Pu

Publication type:

Article

Editorial.

Published in:: Human Heredity, 1999, v. 49, n. 1, p. 1, doi. 10.1159/000022831
Publication type:: Article