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  Human Heredity: Volume 49, Nr. 3, 1999  
  May 31, 1999

virtual library in human genetics and molecular biology

 
     
J. Ott, New York, N.Y.


S. Karger AG
  Date of publishing: May, 1999  
 


Original Paper

Screening for Mutations in the Promoter and the Coding Region of the IGFBP1 and IGFBP3 Genes in Silver-Russell Syndrome Patients
Katja Eggermann, Hartmut A. Wollmann, Jürgen Tomiuk, Michael B. Ranke, Peter Kaiser, Thomas Eggermann

Localization of the Gene Responsible for Familial Benign Polycythemia to Chromosome 11q23
Natalia N. Vasserman, Luisa M. Karzakova, Svetlana M. Tverskaya, Vladimir N. Saperov, Olga M. Muchukova, Galina P. Pavlova, Nadejda K. Efimova, Natalia N. Vankina, Oleg V. Evgrafov

Detection of the Most Common G6PD Gene Mutations in Chinese Using Amplification Refractory Mutation System
Chuan S. Du, Xiaoqin Ren, Luming Chen, Weiying Jiang, Yongshu He, Ming Yang

Simple Tandem Repeat Polymorphisms in the Neuronal Nitric Oxide Synthase Gene in Different Ethnic Populations
Hartmut Grasemann, Jeffrey M. Drazen, Aaron Deykin, Elliot Israel, George T. De Sanctis, Anthony Pillari, Chandri N. Yandava

Analysis of Estrogen Receptor Dinucleotide Polymorphism by Capillary Gel Electrophoresis with a Population Genetic Study in 180 Finns
Tarja A. Kunnas, Doris Holmberg-Marttila, Pekka J. Karhunen

Testing for Linkage under Robust Genetic Models
R. Guerra, Y. Wan, A. Jia, C.I. Amos, J.C. Cohen

The LWb Blood Group as a Marker of Prehistoric Baltic Migrations and Admixture
P. Sistonen, K. Virtaranta-Knowles, R. Denisova, V. Kuinskas, D. Ambrasiene, L. Beckman

Familiality of Quantitative Metabolic Traits in Finnish Families with Non-Insulin-Dependent Diabetes mellitus
Richard M. Watanabe, Timo Valle, Elizabeth R. Hauser, Soumitra Ghosh, Johan Eriksson, Kimmo Kohtamäki, Christian Ehnholm, Jaakko Tuomilehto, Francis S. Collins, Richard N. Bergman, Michael Boehnke, for the Finland-United States Investigation of NIDDM Genetics (FUSION) Study Investigators

Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population:
Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease

M. Natividad Lobato, M. Luisa Ordóñez-Sánchez, M. Teresa Tusié-Luna, Anna Meseguer


Mutation Report

A Novel G to A Substitution at Nucleotide 1734 of the FBN1 Gene Predicting a C534Y Mutation Responsible for Marfan Syndrome
Michael W. Kilpatrick, Peter Lembessis, Elise Rose, Petros Tsipouras


Short Communications

Gln—>Arg 191 Polymorphism of Paraoxonase and Parkinson's Disease
S. Akhmedova, S. Anisimov, A. Yakimovsky, E. Schwartz

New AccI Polymorphism in the Follicle-Stimulating Hormone Beta-Subunit Gene and Its Prevalence in Three Southeast Asian Populations
Wu-Xiang Liao, Yan Tong, Ashim C. Roy, Soon Chye Ng


 
     
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S. KARGER AG, BASEL
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