Results 321 to 330 of about 1,049,137 (382)
Epigenetic mechanisms in maternal-fetal crosstalk: inter- and trans-generational inheritance. [PDF]
EpigenomicsTisato V +6 more
europepmc +1 more source
Rare Dual Genetic Diagnosis of Wiskott-Aldrich Syndrome and Ghoshal Hematodiaphyseal Dysplasia: Clinical, Diagnostic, and Management Challenges. [PDF]
CureusBaby EP +4 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Pleiades: Literature in Context, 2021
Exploring how the U.S. military can move beyond Iraq and AfghanistanSince the September 11, 2001, attacks, the U.S. military has been fighting incessantly in conflicts around the globe, often with inconclusive results.
J. Sanders
semanticscholar +1 more source
Exploring how the U.S. military can move beyond Iraq and AfghanistanSince the September 11, 2001, attacks, the U.S. military has been fighting incessantly in conflicts around the globe, often with inconclusive results.
J. Sanders
semanticscholar +1 more source
Obstetrics and Gynecology Clinics of North America, 2006
Many inherited thrombophilias have been detected and the pathophysiologic insight has increased tremendously during the last decades. Despite, however, the overwhelming observational evidence on the association between inherited thrombophilia and several women's health issues, including VTE, thus far the implications for clinical practice are uncertain.
Coppens, Michiel +2 more
openaire +3 more sources
Many inherited thrombophilias have been detected and the pathophysiologic insight has increased tremendously during the last decades. Despite, however, the overwhelming observational evidence on the association between inherited thrombophilia and several women's health issues, including VTE, thus far the implications for clinical practice are uncertain.
Coppens, Michiel +2 more
openaire +3 more sources
Inherited Macrothrombocytopenias
Seminars in Thrombosis and Hemostasis, 2014Inherited macrothrombocytopenias are a clinically heterogeneous group of disorders, many of which cause moderate-to-severe bleeding tendencies in affected individuals, but which remain under-recognized and are frequently misdiagnosed as immune thrombocytopenia purpura. Diagnostic strategies to date have included a predominant phenotypic approach.
David John, Rabbolini +3 more
openaire +2 more sources