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Vol. 50, No. 4, 2000        July–August 2000 (April 2000)
 

 

Original Paper
211 A Unified Approach to Adjusting Association Tests for Population Admixture with Arbitrary Pedigree Structure and Arbitrary Missing Marker Information
Rabinowitz, D. ;    Laird, N. 
Hum Hered 2000;50:211-223 (DOI:10.1159/000022918)     
Free Abstract     Article (References)     Article (PDF 330 KB)     


224 Apolipoprotein B 3'-VNTR Polymorphism in the Udmurt Population
Spitsyn, V.A. ;    Khorte, M.V. ;    Pogoda, T.V. ;    Slominsky, P.A. ;    Nurbaev, S.D. ;    Agapova, R.K. ;    Limborska, S.A. 
Hum Hered 2000;50:224-226 (DOI:10.1159/000022919)     
Free Abstract     Article (References)     Article (PDF 251 KB)     


227 Adjusting for Confounding due to Population Admixture when Estimating the Effect of Candidate Genes on Quantitative Traits
Yang, Q. ;    Rabinowitz, D. ;    Isasi, C. ;    Shea, S. 
Hum Hered 2000;50:227-233 (DOI:10.1159/000022920)     
Free Abstract     Article (References)     Article (PDF 304 KB)     


234 K5 D328E: A Novel Missense Mutation in the Linker 12 Domain of Keratin 5 Associated with Epidermolysis bullosa simplex (Weber-Cockayne)
Liovic, M. ;    Podrumac, B. ;    Dragos, V. ;    Vouk, K. ;    Komel, R. 
Hum Hered 2000;50:234-236 (DOI:10.1159/000022921)     
Free Abstract     Article (References)     Article (PDF 366 KB)     


237 Molecular Heterogeneity of the Glucose-6-Phosphate Dehydrogenase Deficiency in the Hellenic Population
Menounos, P. ;    Zervas, C. ;    Garinis, G. ;    Doukas, C. ;    Kolokithopoulos, D. ;    Tegos, C. ;    Patrinos, G.P. 
Hum Hered 2000;50:237-241 (DOI:10.1159/000022922)     
Free Abstract     Article (References)     Article (PDF 268 KB)     


242 High Frequency of HLA-DQB1 Non-Asp57 Alleles in Kuwaiti Children with Insulin-Dependent Diabetes mellitus
Haider, M.Z. ;    Shaltout, A. ;    Alsaeid, K. ;    Al-Khawari, M. ;    Dorman, J.S. 
Hum Hered 2000;50:242-246 (DOI:10.1159/000022923)     
Free Abstract     Article (References)     Article (PDF 262 KB)     


247 Identification of a Prevalent Nonsense Mutation (W283X) and Two Novel Mutations in the Porphobilinogen Deaminase Gene of Swiss Patients with Acute Intermittent Porphyria
Schneider-Yin, X. ;    Bogard, C. ;    Rüfenacht, U.B. ;    Puy, H. ;    Nordmann, Y. ;    Minder, E.I. ;    Deybach, J.-C. 
Hum Hered 2000;50:247-250 (DOI:10.1159/000022924)     
Free Abstract     Article (References)     Article (PDF 444 KB)     


251 Linkage Analysis of Quantitative Trait Loci: Sib Pairs or Sibships?
Alcaïs, A. ;    Abel, L. 
Hum Hered 2000;50:251-256 (DOI:10.1159/000022925)     
Free Abstract     Article (References)     Article (PDF 303 KB)     


257 A Study on the Degree of Relationship between Two Individuals
Montes, F. ;    Plaza, M. ;    Ruá, E. 
Hum Hered 2000;50:257-262 (DOI:10.1159/000022926)     
Free Abstract     Article (References)     Article (PDF 481 KB)     


263 Haptoglobin 1F Allele Frequency Is High among Indigenous Populations in the State of Durango, Mexico
Delanghe, J. ;    Langlois, M. ;    Alvarado Esquivel, C. ;    De Haene, H. ;    De Buyzere, M. 
Hum Hered 2000;50:263-265 (DOI:10.1159/000022927)     
Free Abstract     Article (References)     Article (PDF 201 KB)     

Mutation Report
266 A Novel Mutation (2409delT) in Exon 14 of the Factor VIII Gene Causes Severe Haemophilia A
Vidal, F. ;    Farssac, E. ;    Altisent, C. ;    Puig, L. ;    Gallardo, D. 
Hum Hered 2000;50:266-267 (DOI:10.1159/000022928)     
Article (PDF 554 KB)     


268 The 677 CrarrT Mutation in the Methylenetetrahydrofolate Reductase (MTHFR) Gene in Five Chinese Ethnic Groups
Yu, J. ;    Chen, B. ;    Zhang, G. ;    Fu, S. ;    Li, P. 
Hum Hered 2000;50:268-270 (DOI:10.1159/000022929)     
Article (PDF 274 KB)     
 
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