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V Tasic

Showing results (31-40 of 35) with videos related to

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Prilozi|January 31, 2012
Acute Gallbladder Hydrops and Arthritis: unusual initial manifestations of Wilson's Disease (WD): Case ReportZ S Gucev, N Pop-Jordanova, V Calovska, et al.
Balkan Journal of Medical Genetics : BJMG|November 7, 2025
Nephrotic Syndrome Induced by Tiopronin in a Male Patient with CystinuriaV Karanfilovski, A Severova Stojanoska, V Ristovska, et al.
Balkan Journal of Medical Genetics : BJMG|September 17, 2019
Duplication of The <i>SOX3</i> Gene in an Sry-negative 46,XX Male with Associated Congenital Anomalies of Kidneys and the Urinary Tract: Case Report and Review of the LiteratureV Tasic, A Mitrotti, F G Riepe, et al.
Journal of Medical Genetics|November 5, 2002
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing lossE H Stover, K J Borthwick, C Bavalia, et al.
The New England Journal of Medicine|January 8, 2015
TBX6 null variants and a common hypomorphic allele in congenital scoliosisN Wu, X Ming, J Xiao, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Prilozi|January 31, 2012
Acute Gallbladder Hydrops and Arthritis: unusual initial manifestations of Wilson's Disease (WD): Case ReportZ S Gucev, N Pop-Jordanova, V Calovska, et al.
Balkan Journal of Medical Genetics : BJMG|November 7, 2025
Nephrotic Syndrome Induced by Tiopronin in a Male Patient with CystinuriaV Karanfilovski, A Severova Stojanoska, V Ristovska, et al.
Balkan Journal of Medical Genetics : BJMG|September 17, 2019
Duplication of The <i>SOX3</i> Gene in an Sry-negative 46,XX Male with Associated Congenital Anomalies of Kidneys and the Urinary Tract: Case Report and Review of the LiteratureV Tasic, A Mitrotti, F G Riepe, et al.
Journal of Medical Genetics|November 5, 2002
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing lossE H Stover, K J Borthwick, C Bavalia, et al.
The New England Journal of Medicine|January 8, 2015
TBX6 null variants and a common hypomorphic allele in congenital scoliosisN Wu, X Ming, J Xiao, et al.
Pageof 4