L. Taft

发表

Population-based study of congenital heart defects in Down syndrome.

M. Khoury, T. Hassold, S. Freeman, 1998, American journal of medical genetics.

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination.

T. Hassold, M. Petersen, M. Mikkelsen, 1994, Human molecular genetics.

Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II

Neil E. Lamb, Stephanie L. Sherman, Lisa Taft, 1996, Nature Genetics.

Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a spopulation-based case-control study

M. Khoury, T. Hassold, Quanhe Yang, 1999, Genetics in Medicine.

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.

E. Feingold, T. Hassold, G. Karadima, 1997, Human molecular genetics.

Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans.

M Mikkelsen, T. Hassold, G. Karadima, 1998, Human molecular genetics.

Women with a reduced ovarian complement may have an increased risk for a child with Down syndrome.

Quanhe Yang, S. Freeman, L. Taft, 2000, American journal of human genetics.

Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.

W D Flanders, M J Khoury, M. Khoury, 1996, American journal of human genetics.

Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population.

D. Crawford, M. Yeargin-Allsopp, C. Boyle, 1999, American journal of human genetics.

Women’s Attitudes Toward Testing for Fragile X Carrier Status: A Qualitative Analysis

L. Taft, S. Sherman, A. Anido, 2005, Journal of Genetic Counseling.

Prevalence of the fragile X syndrome in African-Americans.

D. Crawford, M. Yeargin-Allsopp, C. Boyle, 2002, American journal of medical genetics.

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.

C. Gunter, A. Reiss, S. Warren, 2000, American journal of human genetics.

FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: no evidence for an increase in aneuploidy

T. Hassold, E. Millie, L. Taft, 1998, Human Genetics.