Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jane Hersey"'
Autor:
Lisa Taft, Dana C. Crawford, James L. Newman, Patricia Holmgreen, Dorothy Pettay, Stephanie L. Sherman, Coleen A. Boyle, Mary L. Stanfield, S. Jane Hersey, Laura B. Gold, Elizabeth F. Hinkle, Marshalyn Yeargin-Allsopp, Kellen L. Meadows
Publikováno v:
The American Journal of Human Genetics. 64(2):495-507
Summary We conducted a large population-based survey of fragile X (FRAXA) syndrome in ethnically diverse metropolitan Atlanta. The eligible study population consisted of public school children, aged 7–10 years, in special education–needs (SEN) cl
Autor:
Michael B. Petersen, Sallie B. Freeman, Anni Hallberg, Yuanchao Gu, Terry J. Hassold, Stephanie L. Sherman, Denise Saker, Margareta Mikkelsen, Dorothy Pettay, Dimitris Avramopoulos, Kristen M. May, Neil E. Lamb, Joseph J. Shen, Amanda Savage-Austin, Jane Hersey, Lisa Taft
Publikováno v:
Nature Genetics. 14:400-405
The cause of non-disjunction of chromosome 21 remains largely unknown. Advanced maternal age is associated with both maternal meiosis I (MI) and meiosis II (MII) non-disjunction events. While reduced genetic recombination has been demonstrated in mat
Autor:
Dorothy Pettay, James L. Newman, Jane Hersey, Kellen L. Meadows, Stephanie L. Sherman, Allison E. Ashley
Publikováno v:
American Journal of Medical Genetics. 64:428-433
To begin to understand the population dynamics of the fragile X (FRAXA) mutation and to learn more about the fragile X E (FRAXE) syndrome, we have initiated a surve of children in special needs education programs in the public school system. With res
Autor:
Sallie B. Freeman, Margareta Mikkelsen, Merete Frantzen, Stephanie L. Sherman, Terry J. Hassold, Michael B. Petersen, Jane Hersey, Dorothy Pettay, Lisa Taft
Publikováno v:
Human Molecular Genetics. 3:1529-1535
Over 300 cases of trisomy 21 were analyzed to characterize the causes of maternal non-disjunction and to evaluate the basis for maternal age-dependent trisomy 21. We confirmed the observation that recombination along 21q is reduced among non-disjoine
Autor:
Georgia Karadima, Sallie B. Freeman, Anni Hallberg, Yuanchao Gu, Dorothy Pettay, Amanda Savage, Margareta Mikkelsen, Neil E. Lamb, Stephanie L. Sherman, Michael B. Petersen, Terry J. Hassold, Jane Hersey, Eleanor Feingold, Dimitris Avramopoulos, Denise Saker, Lisa Taft, Joseph J. Shen
Publikováno v:
Human molecular genetics. 6(9)
Recent studies of trisomy 21 have shown that altered levels of recombination are associated with maternal non-disjunction occurring at both meiosis I (MI) and meiosis II (MII). To comprehend better the association of recombination with nondisjunction