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Results of search for 'au:"Oygar, D Deren"'
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Authors
Connor, Thomas M F
Gale, Daniel P
Hmida, Mohamed Ben
Khan, Nadia
Lapsley, Marta
Levine, Adam P
Lin, Fujun
Maxwell, Patrick H
Neild, Guy H
Nitsch, Dorothea
Oygar, D Deren
Oygar, P Derin
Segal, Anthony W
Steenkamp, Retha
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Topics
Adult
Africa, Northern
Algorithms
Autoantigens
Clinical Coding
Collagen Type IV
Cyprus
DNA
DNA Mutational Analysis
Diabetes Complications
Female
Genetic Linkage
Genotype
Humans
Kidney Diseases
Kidney Failure, Chronic
Male
Middle East
Pedigree
genetics
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English
Your search returned 5 results.
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1.
Can we improve the diagnosis of renal failure? A revised coding system for the Middle East and North Africa.
[electronic resource]
by
Neild, Guy H
Oygar, D Deren
Hmida, Mohamed Ben
Producer:
20110913
In:
Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia
vol. 22
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2.
Can we improve diagnosis of renal failure? A revised coding system for Middle East and North Africa.
[electronic resource]
by
Neild, Guy H
Oygar, D Deren
Hmida, Mohamed Ben
Producer:
20110805
In:
Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia
vol. 22
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No items available.
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3.
Incidence of end-stage renal disease in the Turkish-Cypriot population of Northern Cyprus: a population based study.
[electronic resource]
by
Connor, Thomas M F
Oygar, D Deren
Gale, Daniel P
Steenkamp, Retha
Nitsch, Dorothea
Neild, Guy H
Maxwell, Patrick H
Producer:
20130719
In:
PloS one
vol. 8
Online resources:
Available from publisher's website
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No items available.
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4.
Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.
[electronic resource]
by
Levine, Adam P
Connor, Thomas M F
Oygar, D Deren
Neild, Guy H
Segal, Anthony W
Maxwell, Patrick H
Gale, Daniel P
Producer:
20150825
In:
BMC genomics
vol. 16
Online resources:
Available from publisher's website
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5.
A novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagen.
[electronic resource]
by
Gale, Daniel P
Oygar, D Deren
Lin, Fujun
Oygar, P Derin
Khan, Nadia
Connor, Thomas M F
Lapsley, Marta
Maxwell, Patrick H
Neild, Guy H
Producer:
20170913
In:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
vol. 31
Online resources:
Available from publisher's website
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