Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kayla M. Sheets"'
Autor:
Michael L. Baird, D. Barry Starr, Debra Davis, Mary E. Sabatini, Kayla M. Sheets, Julie Heinig
Publikováno v:
Journal of Assisted Reproduction and Genetics
In the fertility clinic setting, a negative DNA paternity test result usually suggests a sample mix-up likely occurred at the testing company or in the clinic. However, we report a case where, despite repeat negative paternity test results, the alleg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f38e10ded980cbe3c21dd682dc106b98
http://europepmc.org/articles/PMC5845036
http://europepmc.org/articles/PMC5845036
Autor:
Derek L. Stirewalt, Steven J. Kussick, Kayla M. Sheets, Era L. Pogosova-Agadjanyan, Cheryl L. Willman, Jerald P. Radich, Soheil Meshinchi
Publikováno v:
British Journal of Haematology. 124:481-484
Internal tandem duplications in FLT3 are the most common mutation in acute myeloid leukaemia (AML), with agarose gel electrophoresis of polymerase chain reaction products (PCR/agarose) being the screening method of choice for these mutations. As PCR/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0eec563f3911fa15e05546515602400
https://doi.org/10.1111/j.1365-2141.2004.04808.x
https://doi.org/10.1111/j.1365-2141.2004.04808.x
Publikováno v:
Journal of genetic counseling. 21(4)
Giving difficult news to patients represents a common dilemma for health care professionals. Based on three decades of research, various authors have proposed guidelines outlining the ideal setting, delivery, and timing. Existing publications focus o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7afba2de5ddcd4d66ff0be3e489c29a2
https://pubmed.ncbi.nlm.nih.gov/22147086
https://pubmed.ncbi.nlm.nih.gov/22147086
Autor:
Derek L, Stirewalt, Soheil, Meshinchi, Steven J, Kussick, Kayla M, Sheets, Era, Pogosova-Agadjanyan, Cheryl L, Willman, Jerald P, Radich
Publikováno v:
British journal of haematology. 124(4)
Internal tandem duplications in FLT3 are the most common mutation in acute myeloid leukaemia (AML), with agarose gel electrophoresis of polymerase chain reaction products (PCR/agarose) being the screening method of choice for these mutations. As PCR/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b369064ed52fae1a8685dd4c5a590931
https://pubmed.ncbi.nlm.nih.gov/14984498
https://pubmed.ncbi.nlm.nih.gov/14984498