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Human Genetics|August 21, 2001
The polyglutamine motif is highly conserved at the Clock locus in various organisms and is not polymorphic in humansQ Saleem, A Anand, S Jain, et al.
Human Genetics|August 21, 2001
Recombination in the pseudoautosomal region in a 47,XYY maleR H Martin, Q Shi, L L Field
Human Genetics|August 21, 2001
Expression pattern, genomic structure and evaluation of the human SLC30A4 gene as a candidate for acrodermatitis enteropathicaS Küry, M C Devilder, H Avet-Loiseau, et al.
Human Genetics|August 21, 2001
A second case of somatic triple mosaicism in the CYBB gene causing chronic granulomatous diseaseD Noack, P G Heyworth, W Kyono, et al.
Human Genetics|July 18, 1979
Associations between atopic diseases and the polymorphic systems ABO, Kidd, Inv and red cell acid phosphataseR Brachtel, H Walter, W Beck, et al.
Human Genetics|June 21, 2001
Oto-facio-cervical (OFC) syndrome is a contiguous gene deletion syndrome involving EYA1: molecular analysis confirms allelism with BOR syndrome and further narrows the Duane syndrome critical region to 1 cMS Rickard, M Parker, W van't Hoff, et al.
Human Genetics|April 3, 2001
Numerical chromosome abnormalities in the spermatozoa of the fathers of children with trisomy 21 of paternal origin: generalised tendency to meiotic non-disjunctionS R Soares, C Templado, J Blanco, et al.
Human Genetics|August 14, 2001
Interaction between the melanocortin-1 receptor and P genes contributes to inter-individual variation in skin pigmentation phenotypes in a Tibetan populationJ M Akey, H Wang, M Xiong, et al.
Human Genetics|August 14, 2001
Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical regionC Braybrook, G Warry, G Howell, et al.
Human Genetics|July 11, 2002
CYP3A4-V and prostate cancer in African Americans: causal or confounding association because of population stratification?Rick A Kittles, Weidong Chen, Ramesh K Panguluri, et al.
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