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Prenatal Diagnosis
|
February 5, 2008
Noninvasive genotyping fetal Kell blood group (KEL1) using cell-free fetal DNA in maternal plasma by MALDI-TOF mass spectrometry
Ying Li, Kirstin Finning, Geoff Daniels, et al.
BMJ (Clinical Research Ed.)
|
April 9, 2008
Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: prospective feasibility study
Kirstin Finning, Pete Martin, Joanna Summers, et al.
Transfusion
|
August 5, 2005
Molecular basis of the JAHK (RH53) antigen
Erwin A Scharberg, Carole Green, Geoff Daniels, et al.
Haematologica
|
April 10, 2010
The majority of the in vitro erythroid expansion potential resides in CD34(-) cells, outweighing the contribution of CD34(+) cells and significantly increasing the erythroblast yield from peripheral blood samples
Emile van den Akker, Timothy J Satchwell, Stephanie Pellegrin, et al.
British Journal of Haematology
|
June 10, 2008
New mutations in C1GALT1C1 in individuals with Tn positive phenotype
Vanja Karamatic Crew, Belinda K Singleton, Carole Green, et al.
Psychiatric Genetics
|
November 30, 2005
McLeod syndrome: life-long neuropsychiatric disorder due to a novel mutation of the XK gene
Adam Zeman, Geoff Daniels, Louise Tilley, et al.
BMJ (Clinical Research Ed.)
|
September 6, 2014
Diagnostic accuracy of routine antenatal determination of fetal RHD status across gestation: population based cohort study
Lyn S Chitty, Kirstin Finning, Angela Wade, et al.
The Journal of Biological Chemistry
|
September 20, 2002
AQP3 deficiency in humans and the molecular basis of a novel blood group system, GIL
Nathalie Roudier, Pierre Ripoche, Pierre Gane, et al.
Gastroenterology
|
July 10, 2002
Altered expression and allelic association of the hypervariable membrane mucin MUC1 in Helicobacter pylori gastritis
Lynne E Vinall, Marie King, Marco Novelli, et al.
Transfusion
|
February 27, 2007
Different inactivating mutations in the LU genes of three individuals with the Lutheran-null phenotype
Vanja Karamatic Crew, Gary Mallinson, Carole Green, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 43) with videos related to
Sort By:
Page
of 5
Prenatal Diagnosis
|
February 5, 2008
Noninvasive genotyping fetal Kell blood group (KEL1) using cell-free fetal DNA in maternal plasma by MALDI-TOF mass spectrometry
Ying Li, Kirstin Finning, Geoff Daniels, et al.
BMJ (Clinical Research Ed.)
|
April 9, 2008
Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: prospective feasibility study
Kirstin Finning, Pete Martin, Joanna Summers, et al.
Transfusion
|
August 5, 2005
Molecular basis of the JAHK (RH53) antigen
Erwin A Scharberg, Carole Green, Geoff Daniels, et al.
Haematologica
|
April 10, 2010
The majority of the in vitro erythroid expansion potential resides in CD34(-) cells, outweighing the contribution of CD34(+) cells and significantly increasing the erythroblast yield from peripheral blood samples
Emile van den Akker, Timothy J Satchwell, Stephanie Pellegrin, et al.
British Journal of Haematology
|
June 10, 2008
New mutations in C1GALT1C1 in individuals with Tn positive phenotype
Vanja Karamatic Crew, Belinda K Singleton, Carole Green, et al.
Psychiatric Genetics
|
November 30, 2005
McLeod syndrome: life-long neuropsychiatric disorder due to a novel mutation of the XK gene
Adam Zeman, Geoff Daniels, Louise Tilley, et al.
BMJ (Clinical Research Ed.)
|
September 6, 2014
Diagnostic accuracy of routine antenatal determination of fetal RHD status across gestation: population based cohort study
Lyn S Chitty, Kirstin Finning, Angela Wade, et al.
The Journal of Biological Chemistry
|
September 20, 2002
AQP3 deficiency in humans and the molecular basis of a novel blood group system, GIL
Nathalie Roudier, Pierre Ripoche, Pierre Gane, et al.
Gastroenterology
|
July 10, 2002
Altered expression and allelic association of the hypervariable membrane mucin MUC1 in Helicobacter pylori gastritis
Lynne E Vinall, Marie King, Marco Novelli, et al.
Transfusion
|
February 27, 2007
Different inactivating mutations in the LU genes of three individuals with the Lutheran-null phenotype
Vanja Karamatic Crew, Gary Mallinson, Carole Green, et al.
Page
of 5