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Human Genetics|January 1, 1991
PAH 399 GTA (Val)----GTT(Val), a new silent mutation found in the ChineseS Z Huang, Z R Ren, Y T Zeng, et al.
Human Genetics|January 1, 1991
Structural organization and polymorphism of the alpha satellite DNA sequences of chromosomes 13 and 21 as revealed by pulse field gel electrophoresisB Marçais, M Bellis, A Gérard, et al.
Human Genetics|January 1, 1991
Allelic somatic mutations may explain vascular twin neviR Happle
Human Genetics|January 1, 1991
Type III hyperlipoproteinemia in a patient with idiopathic hemochromatosisG Feussner, R Ziegler
Human Genetics|February 1, 1991
Duplication of exons 13, 14 and 15 of the LDL-receptor gene in a patient with heterozygous familial hypercholesterolemiaN Lelli, M Ghisellini, S Calandra, et al.
Human Genetics|February 1, 1991
Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23A Caiulo, S Nicolis, P Bianchi, et al.
Human Genetics|February 1, 1991
Identification of a cystic fibrosis mutation: deletion of isoleucine506P V Nelson, W F Carey, C P Morris
Human Genetics|February 1, 1991
Incidence of Menkes diseaseT Tønnesen, W J Kleijer, N Horn
Human Genetics|February 1, 1991
Physical mapping of two Xp markers DXS16 and DXS143U Thies, V V Rao, W Engel, et al.
Human Genetics|November 17, 2009
Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aboriginesHung-Pin Tu, Albert Min-Shan Ko, Shu-Jung Wang, et al.
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