The timing of twinning: more insights from X inactivation. Read more about The timing of twinning: more insights from X inactivation.
DAX1 mutations map to putative structural domains in a deduced three-dimensional model. Read more about DAX1 mutations map to putative structural domains in a deduced three-dimensional model.
The gene for severe combined immunodeficiency disease in Athabascan-speaking Native Americans is located on chromosome 10p. Read more about The gene for severe combined immunodeficiency disease in Athabascan-speaking Native Americans is located on chromosome 10p.
Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2q24. Read more about Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2q24.
Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer. Read more about Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer.
Segregation analysis of cryptogenic epilepsy and an empirical test of the validity of the results. Read more about Segregation analysis of cryptogenic epilepsy and an empirical test of the validity of the results.
Mapping quantitative-trait loci in humans by use of extreme concordant sib pairs: selected sampling by parental phenotypes. Read more about Mapping quantitative-trait loci in humans by use of extreme concordant sib pairs: selected sampling by parental phenotypes.
Mapping quantitative trait loci with extreme discordant sib pairs: sampling considerations. Read more about Mapping quantitative trait loci with extreme discordant sib pairs: sampling considerations.
PRB1, PRB2, and PRB4 coded polymorphisms among human salivary concanavalin-A binding, II-1, and Po proline-rich proteins. Read more about PRB1, PRB2, and PRB4 coded polymorphisms among human salivary concanavalin-A binding, II-1, and Po proline-rich proteins.
Two mutational hotspots in the interleukin-2 receptor gamma chain gene causing human X-linked severe combined immunodeficiency. Read more about Two mutational hotspots in the interleukin-2 receptor gamma chain gene causing human X-linked severe combined immunodeficiency.
