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virtual library in human genetics and molecular biology

Original Papers
A Unified Approach to Adjusting Association Tests for Population Admixture with Arbitrary Pedigree Structure and Arbitrary Missing Marker Information
Rabinowitz, D. (New York, N.Y.); Laird, N. (Boston, Mass.)

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. (Moscow)

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. (New York, N.Y.)

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. (Ljubljana)

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. (Athens); Patrinos, G.P. (Athens/Rotterdam)

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. (Kuwait); Dorman, J.S. (Pittsburg, Pa.)

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. (Zürich); Bogard, C. (Colombes); Rüfenacht, U.B. (Zürich); Puy, H.; Nordmann, Y. (Colombes); Minder, E.I. (Zürich); Deybach, J.-C. (Colombes)

Linkage Analysis of Quantitative Trait Loci: Sib Pairs or Sibships?
Alcaïs, A.; Abel, L. (Paris)

A Study on the Degree of Relationship between Two Individuals
Montes, F. (Burjassot); Plaza, M. (Cindad Real); Ruá, E. (Burjassot)

Haptoglobin 1F Allele Frequency Is High among Indigenous Populations in the State of Durango, Mexico
Delanghe, J.; Langlois, M. (Gent); Alvarado Esquivel, C. (Durango); De Haene, H.; De Buyzere, M. (Gent)

Mutation Reports
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. (Barcelona)

The 677 C T Mutation in the Methylenetetrahydrofolate Reductase (MTHFR) Gene in Five Chinese Ethnic Groups
Yu, J.; Chen, B.; Zhang, G.; Fu, S.; Li, P. (Harbin)

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