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P Warwicker

Showing results (11-20 of 15) with videos related to

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Prenatal Diagnosis|October 1, 1996
Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardationA L Webb, S Sturgiss, P Warwicker, et al.
Journal of Medical Virology|April 1, 1996
"Cytomegalovirus disease" in renal allograft recipients: is human herpesvirus 7 a co-factor for disease progression?H K Osman, J S Peiris, C E Taylor, et al.
Kidney International|April 29, 1998
Genetic studies into inherited and sporadic hemolytic uremic syndromeP Warwicker, T H Goodship, R L Donne, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 27, 1999
Familial relapsing haemolytic uraemic syndrome and complement factor H deficiencyP Warwicker, R L Donne, J A Goodship, et al.
American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Prenatal Diagnosis|October 1, 1996
Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardationA L Webb, S Sturgiss, P Warwicker, et al.
Journal of Medical Virology|April 1, 1996
"Cytomegalovirus disease" in renal allograft recipients: is human herpesvirus 7 a co-factor for disease progression?H K Osman, J S Peiris, C E Taylor, et al.
Kidney International|April 29, 1998
Genetic studies into inherited and sporadic hemolytic uremic syndromeP Warwicker, T H Goodship, R L Donne, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 27, 1999
Familial relapsing haemolytic uraemic syndrome and complement factor H deficiencyP Warwicker, R L Donne, J A Goodship, et al.
American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.
Pageof 2