Absence of the derived allele at the DYS199 locus in 3 NE Chinese populationsWANG, B.-Q; FU, S.-B; SUN, Y.-Y et al.Human heredity. 1999, Vol 49, Num 1, pp 63-64, issn 0001-5652Article

Allele frequencies in a worldwide survey of a CA repeat in the first intron of the CFTR geneMATEU, E; CALAFELL, F; BONNE-TAMIR, B et al.Human heredity. 1999, Vol 49, Num 1, pp 15-20, issn 0001-5652Article

Genomic distribution and gonadal mRNA expression of two human luteinizing hormone receptor exon 1 sequences in random populationsTSAI-MORRIS, C. H; YI GENG; BUCZKO, E et al.Human heredity. 1999, Vol 49, Num 1, pp 48-51, issn 0001-5652Article

Identification in Portugal and Brazil of a mtDNA lineage containing a 9-bp triplication of the intergenic coII/tRNA^Lys regionALVES-SILVA, J; GUIMARAES, P. E. M; ROCHA, J et al.Human heredity. 1999, Vol 49, Num 1, pp 56-58, issn 0001-5652Article

Population study of common glucose-6-phosphate dehydrogenase mutations in KuwaitSAMILCHUK, E; D'SOUZA, B; AL-AWADI, S et al.Human heredity. 1999, Vol 49, Num 1, pp 41-44, issn 0001-5652Article

Variable distribution of TFF2 (spasmolysin) alleles in Europeans does not indicate predisposition to gastric cancerDOS SANTOS SILVA, E; KAYADEMIR, T; REGATEIRO, F et al.Human heredity. 1999, Vol 49, Num 1, pp 45-47, issn 0001-5652Article

α₁-Antitrypsin (PI) alleles as markers of Westeuropean influence in the Baltic Sea regionBECKMAN, L; SIKSTRÖM, C; MIKELSAAR, A.-V et al.Human heredity. 1999, Vol 49, Num 1, pp 52-55, issn 0001-5652Article

HpaII polymerase chain reaction restriction fragment length polymorphism in the human CD19 gene on 16p11THUNBERG, U; GIDLÖF, C; BANGHAGEN, M et al.Human heredity. 1998, Vol 48, Num 4, pp 230-231, issn 0001-5652Article

¹⁶⁰Thr mutation in the rhodopsin gene associated with retinitis pigmentosaCAPEANS, C; BLANCO, M. J; LAREU, M. V et al.Human heredity. 1998, Vol 48, Num 5, pp 237-240, issn 0001-5652Article

Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21NANCE, M. A; RAABE, W. A; MIDANI, H et al.Human heredity. 1998, Vol 48, Num 3, pp 169-178, issn 0001-5652Article

DNA analysis of the fragile X syndrome in an at risk pediatric population in Croatia : Simple clinical preselection criteria can considerably improve the cost-effectiveness of fragile X screening studiesHECIMOVIC, S; BARISIC, I; PAVELIC, K et al.Human heredity. 1998, Vol 48, Num 5, pp 256-265, issn 0001-5652Article

Genetic relationships among Japanese, Northern Han, Hui, Uygur, Kazakh, Greek, Saudi Arabian, and Italian populations based on allelic frequencies at four VNTR (D1S80, D4S43, COL2A1, D17S5) and one STR (ACTBP2) lociKATSUYAMA, Y; INOKO, H; IMANISHI, T et al.Human heredity. 1998, Vol 48, Num 3, pp 126-137, issn 0001-5652Article

Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from SlovakiaPLASILOVA, M; FERAKOVA, E; KADASI, L et al.Human heredity. 1998, Vol 48, Num 1, pp 30-33, issn 0001-5652Article

Transferrin variants as markers of migrations and admixture between populations in the Baltic Sea regionBECKMAN, L; SIKSTRÖM, C; MIKELSAAR, A.-V et al.Human heredity. 1998, Vol 48, Num 4, pp 185-191, issn 0001-5652Article

A novel missense mutation D676N in the plasminogen gene causes loss of functional activityYAMAGUCHI, M; SUGIYAMA, S; NODA, H et al.Human heredity. 1997, Vol 47, Num 4, pp 234-236, issn 0001-5652Article

Data on six short-tandem repeat polymorphisms in an autochthonous Basque populationIRIONDO, M; BARBERO, M. C; IZAGIRRE, N et al.Human heredity. 1997, Vol 47, Num 3, pp 131-137, issn 0001-5652Article

Haptoglobin polymorphism in Korean patients with cardiovascular diseasesSEUNG HO HONG; BYUNG YONG KANG; JEOM HEE LIM et al.Human heredity. 1997, Vol 47, Num 5, pp 283-287, issn 0001-5652Article

Is cellulose acetate electrophoresis a suitable technique for detection of Hb Bart's at birth ?DESAI, S; COLAH, R; GUPTE, S et al.Human heredity. 1997, Vol 47, Num 4, pp 181-184, issn 0001-5652Article

Phenylketonuria mutations and linked haplotypes in the Lithuanian population : Origin of the most common R408W mutationGIANNATTASIO, S; JURGELEVICIUS, V; LATTANZIO, P et al.Human heredity. 1997, Vol 47, Num 3, pp 155-160, issn 0001-5652Article

Population studies of human deoxyribonuclease I polymorphismYASUDA, T; TAKESHITA, H; IIDA, R et al.Human heredity. 1997, Vol 47, Num 3, pp 121-124, issn 0001-5652Article

The spectrum of beta-thalassaemia mutations in the LebanonZAHED, L; TALHOUK, R; SALEH, M et al.Human heredity. 1997, Vol 47, Num 5, pp 241-249, issn 0001-5652Article

AvaI polymorphism in the human transferrin geneTSUCHIDA, S; IKEMOTO, S; KAJII, E et al.Human heredity. 1997, Vol 47, Num 6, pp 338-341, issn 0001-5652Article

Consanguinity and associated socio-demographic factors in the United Arab EmiratesBENER, A; ABDULRAZZAQ, Y. M; AL-GAZALI, L. I et al.Human heredity. 1996, Vol 46, Num 5, pp 256-264, issn 0001-5652Article

Familial aggregation studies with matched proband samplingWILLIAMSON, J; TOSTESON, T; REDLINE, S et al.Human heredity. 1996, Vol 46, Num 2, pp 76-84, issn 0001-5652Article

Interpopulational and intrapopulational genetic diversity of Amerindians as revealed by six variable number of tandem repeatsZAGO, M. A; SILVA, W. A; TAVELLA, M. H et al.Human heredity. 1996, Vol 46, Num 5, pp 274-289, issn 0001-5652Article