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Results: 1-6 |
Results: 6
Estimation of morbid risk and age at onset with missing information.
Authors: Cupples, L. Adrienne Risch, Neil Farrer, Lindsay A. Myers, Richard H.
Citation: Cupples, L. Adrienne et al., Estimation of morbid risk and age at onset with missing information., American journal of human genetics , 49-I(1), 1991, pp. 76-87
Inverse relationship between age at onset of Huntington disease and paternal age suggests involvement of genetic imprinting.
Authors: Farrer, Lindsay A. Cupples, L. Adrienne Kiely, Dan K. Conneally, Michael Myers, Richard H.
Citation: A. Farrer, Lindsay et al., Inverse relationship between age at onset of Huntington disease and paternal age suggests involvement of genetic imprinting., American journal of human genetics , 50-I(3), 1992, pp. 528-535
A test of the hypothesis that age at onset in Huntington disease is controlled by an X-linked recessive modifier.
Authors: Ridley, Rosalind M Farrer, Lindsay A. Frith, Chris D. Conneally, P. Michael
Citation: M. Ridley, Rosalind et al., A test of the hypothesis that age at onset in Huntington disease is controlled by an X-linked recessive modifier., American journal of human genetics , 50-I(3), 1992, pp. 536-543
Homozygote for huntington disease
Authors: Myers, Richard H. Leavitt, Julie Farrer, Lindsay A. Jagadeesh, Jaya McFarlane, Heather Mastromauro, Carol A. Mark, Raymond J. Gusella, James F.
Citation: H. Myers, Richard et al., Homozygote for huntington disease, American journal of human genetics , 45-I(4), 1989, pp. 615-618
Waardenberg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS consortium
Authors: Farrer, Lindsay A. Grundfast, Kenneth M Amos, Jean Arnos, Kathleen S. Asher, James H. Beighton, Peter Diehl, Scott R. Fex, Jörgen Foy, Carole Friedman, Thomas B. Greenberg, Jacquie Hoth, Christopher Marazita, Mary Milunsky, Aubrey Morell, Robert Nance, Walter Newton, Valerie Ramesar, Rajkumar San Agustin, Theresa B. Skare, James Stevens, Cathy A. Wagner, Ronald G. Wilcox,Edward R. Winship, Ingrid Read, Andrew P.
Citation: A. Farrer, Lindsay et al., Waardenberg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS consortium, American journal of human genetics , 50-II(5), 1992, pp. 902-913
Segregation analysis reveals evidence of a major gene for Alzheimer disease.
Authors: Farrer, Lindsay A. Myers, Richard H. Connor, Linda Cupples, L. Adrienne Growdon, John H.
Citation: A. Farrer, Lindsay et al., Segregation analysis reveals evidence of a major gene for Alzheimer disease., American journal of human genetics , 48-II(6), 1991, pp. 1026-1033
Risultati: 1-6 |