نتایج جستجو برای: familial characteristics

تعداد نتایج: 713247  

Journal: :Twin research : the official journal of the International Society for Twin Studies 2003
Alun Evans G Caroline M Van Baal Peter McCarron Marlies DeLange Thorkild I Soerensen Eco J C De Geus Kirsten Kyvik Nancy L Pedersen Tim D Spector Toby Andrew Christopher Patterson John B Whitfield Gu Zhu Nicholas G Martin Jaakko Kaprio Dorret I Boomsma

Despite the decline in coronary heart disease in many European countries, the disease remains an enormous public health problem. Although we know a great deal about environmental risk factors for coronary heart disease, a heritable component was recognized a long time ago. The earliest and best known examples of how our genetic constitution may determine cardiovascular risk relate to lipoprotei...

Journal: :American journal of clinical pathology 2007
Patricia Aoun Guimei Zhou Wing C Chan Cynthia Page Kellie Neth Diane Pickering Warren Sanger Brigid Quinn-Laquer Patrice Watson Jane F Lynch Henry T Lynch Dennis D Weisenburger

B-cell chronic lymphocytic leukemia (B-CLL) is a heterogeneous disease that may exhibit familial clustering. We examined the cytogenetic, immunophenotypic, and VH gene usage characteristics of a family with B-CLL affecting 7 members in 3 generations. Interphase fluorescence in situ hybridization studies identified an acquired deletion of chromosome 13q14 in the leukemic cells of 6 affected memb...

Journal: :Neurologic clinics 2007
James L Fisher Judith A Schwartzbaum Margaret Wrensch Joseph L Wiemels

Brain tumors seemed to have increased in incidence over the past 30 years, but the rise probably results from use of new neuroimaging techniques. Treatments have not improved prognosis for rapidly fatal brain tumors. Established brain tumor risk factors (exposure to ionizing radiation, rare mutations of penetrant genes, and familial history) explain only a small proportion of brain tumors, and ...

2014
Xiuhua Ding Shaoyong Su Kannabiran Nandakumar Xiaoling Wang David W Fardo

Large-scale genetic studies are often composed of related participants, and utilizing familial relationships can be cumbersome and computationally challenging. We present an approach to efficiently handle sequencing data from complex pedigrees that incorporates information from rare variants as well as common variants. Our method employs a 2-step procedure that sequentially regresses out correl...

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