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American Journal of Human Genetics|May 1, 1997
The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human developmentS Gottlieb, B S Emanuel, D A Driscoll, et al.American Journal of Human Genetics|May 1, 1997
The likelihood of being affected with Huntington disease by a particular age, for a specific CAG sizeR R Brinkman, M M Mezei, J Theilmann, et al.American Journal of Human Genetics|May 1, 1997
Cost-effective sib-pair designs in the mapping of quantitative-trait lociH Zhao, H Zhang, J I RotterAmerican Journal of Human Genetics|May 1, 1997
Optimal strategies for mapping complex diseases in the presence of multiple lociD E Goldgar, D F EastonAmerican Journal of Human Genetics|October 3, 1998
Mixed messages: presentation of information in cystic fibrosis-screening pamphletsG L Loeben, T M Marteau, B S WilfondAmerican Journal of Human Genetics|October 3, 1998
A chromosomal deletion map of human malformationsC Brewer, S Holloway, P Zawalnyski, et al.American Journal of Human Genetics|October 3, 1998
Prenatal screening for cystic fibrosis carriers: an economic evaluationP T Rowley, S Loader, R M KaplanAmerican Journal of Human Genetics|October 3, 1998
Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)C Donger, E Krejci, A P Serradell, et al.American Journal of Human Genetics|October 3, 1998
Attitudes of deaf adults toward genetic testing for hereditary deafnessA Middleton, J Hewison, R F MuellerAmerican Journal of Human Genetics|October 3, 1998
Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24G C Fong, P U Shah, M N Gee, et al.Pageof 979