Low frequency of CYP21B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyBACHEGA, T. A. S. S; BILLERBECK, A. E. C; MADUREIRA, G et al.Human heredity. 1999, Vol 49, Num 1, pp 9-14, issn 0001-5652Article

A novel in frame deletion of codons 188-190 in the hMSH2 gene of a Slovenian patient with hereditary non-polyposis colorectal cancerRAVNIK-GLAVAC, M; POTOCNIK, U; KOZELJ, M et al.Human heredity. 1998, Vol 48, Num 5, pp 285-287, issn 0001-5652Article

A novel mutation Q602STOP in exon 12 of the FVIII geneSTRMECKI, L; BENEDIK-DOLNICAR, M; KOMEL, R et al.Human heredity. 1998, Vol 48, Num 2, pp 119-120, issn 0001-5652Article

Adult-onset primary open angle glaucoma does not localize to chromosome 2cen-q13 in North American familiesALLINGHAM, R. R; WIGGS, J. L; PERICAK-VANCE, M. A et al.Human heredity. 1998, Vol 48, Num 5, pp 251-255, issn 0001-5652Article

Extreme selection strategies in gene mapping studies of oligogenic quantitative traits do not always increase powerALLISON, D. B; HEO, M; SCHORK, N. J et al.Human heredity. 1998, Vol 48, Num 2, pp 97-107, issn 0001-5652Article

Generating consistent genotypic configurations for multi-allelic loci and large complex pedigreesHEATH, S. C.Human heredity. 1998, Vol 48, Num 1, pp 1-11, issn 0001-5652Article

No evidence for an association between a variant of the mast cell chymase gene and atopic dermatitis based on case-control and haplotype-relative-risk analysesKAWASHIMA, T; NOGUCHI, E; ARINAMI, T et al.Human heredity. 1998, Vol 48, Num 5, pp 271-274, issn 0001-5652Article

The genetic polymorphism of aminolevulinate dehydratase (ALADH) in GreeceKAPOTIS, C; TSOMI, A; BABIONITAKIS, A et al.Human heredity. 1998, Vol 48, Num 3, pp 155-157, issn 0001-5652Article

Genetic polymorphisms of apolipoproteins A-IV, E and H in KoreansHYUN SUP KIM; KAMBOH, M. I.Human heredity. 1998, Vol 48, Num 6, pp 313-317, issn 0001-5652Article

The power of linkage detection by the transmission/disequilibrium testsMOMIAO XIONG; GUO, S.-W.Human heredity. 1998, Vol 48, Num 6, pp 295-312, issn 0001-5652Article

A faster and more general hidden Markov model algorithm for multipoint likelihood calculationsIDURY, R. M; ELSTON, R. C.Human heredity. 1997, Vol 47, Num 4, pp 197-202, issn 0001-5652Article

Congenital anomalies in infants with congenital hypothyroidism : Is it a coincidental or an associated finding ?AL-JURAYYAN, N. A. M; AL-HERBISH, A. S; EL-DESOUKI, M. I et al.Human heredity. 1997, Vol 47, Num 1, pp 33-37, issn 0001-5652Article

Distribution of apolipoprotein E gene polymorphisms in Japanese patients with Alzheimer's disease and in Japanese centenariansYAMAGATA, Z; ASADA, T; KINOSHITA, A et al.Human heredity. 1997, Vol 47, Num 1, pp 22-26, issn 0001-5652Article

Maternal inheritance of atopy at the FcεRIβ locus in Japanese sibsMAO, X.-Q; SHIRAKAWA, T; SASAKI, S et al.Human heredity. 1997, Vol 47, Num 3, pp 178-180, issn 0001-5652Article

Trade-off between sibship size and sampling scheme for detecting quantitative trait lociTODOROV, A. A; PROVINCE, M. A; BORECKI, I. B et al.Human heredity. 1997, Vol 47, Num 1, pp 1-5, issn 0001-5652Article

A transmission disequilibrium test for quantitative trait lociRABINOWITZ, D.Human heredity. 1997, Vol 47, Num 6, pp 342-350, issn 0001-5652Article

Estimating the age of mutant disease alleles based on linkage disequilibriumGUO, S.-W; XIONG, M.Human heredity. 1997, Vol 47, Num 6, pp 315-337, issn 0001-5652Article

Feasibility of collecting disease reports from relatives for genetic epidemiologic investigationsROMITTI, P. A; BURNS, T. L.Human heredity. 1997, Vol 47, Num 6, pp 351-357, issn 0001-5652Article

Linkage disequilibrium measures for fine-scale mapping : A comparisonGUO, S.-W.Human heredity. 1997, Vol 47, Num 6, pp 301-314, issn 0001-5652Article

Association between the p21 codon 31 A1 (arg) allele and lung cancerSJÄLANDER, A; BIRGANDER, R; RANNUG, A et al.Human heredity. 1996, Vol 46, Num 4, pp 221-225, issn 0001-5652Article

Coagulation factor XIIIA subtypes in Brazilian IndiansARNOLD, G; KÖMPF, J; SALZANO, F. M et al.Human heredity. 1996, Vol 46, Num 3, pp 132-135, issn 0001-5652Article

Detection of the plasma cholinesterase K variant by PCR using an amplification-created restriction siteJENSEN, F. S; NIELSEN, L. R; SCWARTZ, M et al.Human heredity. 1996, Vol 46, Num 1, pp 26-31, issn 0001-5652Article

Distribution of composite CYP1A1 genotypes in Africans, African-Americans and CaucasiansGARTE, S. J; TRACHMAN, J; CROFTS, F et al.Human heredity. 1996, Vol 46, Num 3, pp 121-127, issn 0001-5652Article

G6PD NanKang (517T→C; 173 Phe→Leu) : A new Chinese G6PD variant associated with neonatal jaundiceCHEN, H.-L; HUANG, M.-J; HUANG, C.-S et al.Human heredity. 1996, Vol 46, Num 4, pp 201-204, issn 0001-5652Article

Lod score curves for phase-unknown matingsHULBERT-SHEARON, T; BOEHNKE, M; LANGE, K et al.Human heredity. 1996, Vol 46, Num 1, pp 55-57, issn 0001-5652Article