Heritability Estimates of Transformations of Normally Distributed Records (1991)
DeStefano, A. L., Van Vleck, L. Dale
Milk yields were simulated for identical twin and parent-progeny pairs to determine effect of transformations on genetic variance. Use of identical twin pairs excludes variability due to Mendelian...
Jiang, Y., Wilk, J. B., Borecki, I., Williamson, S., DeStefano, A. L., Xu, G., ...
Linkage of body mass index (BMI) to a broad region of chromosome 7q22-35 has been reported in multiple studies. We previously published a multipoint LOD score of 4.9 at D7S1804 for BMI from the...
Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q.
DeStefano, A L, Baldwin, C T, Burzstyn, M, Gavras, I, Handy, D E, Joost, O, ...
Familial orthostatic hypotensive disorder is characterized by light-headedness on standing, which may worsen to syncope, palpitations, and blue-purple ankle discoloration, and is accompanied by a...
Jiang, Y., Wilk, J. B., Borecki, I., Williamson, S., DeStefano, A. L., Xu, G., ...
Linkage of body mass index (BMI) to a broad region of chromosome 7q22-35 has been reported in multiple studies. We previously published a multipoint LOD score of 4.9 at D7S1804 for BMI from the...
Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q.
DeStefano, A L, Baldwin, C T, Burzstyn, M, Gavras, I, Handy, D E, Joost, O, ...
Familial orthostatic hypotensive disorder is characterized by light-headedness on standing, which may worsen to syncope, palpitations, and blue-purple ankle discoloration, and is accompanied by a...
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.
Bonné-Tamir, B., DeStefano, A. L., Briggs, C. E., Adair, R., Franklyn, B., Weiss, S., ...
Deafness is a heterogeneous trait affecting approximately 1/1,000 newborns. Genetic linkage studies have already implicated more than a dozen distinct loci causing deafness. We conducted a genome...