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Townes–Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family

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Bibliographic Details
Published in:Balkan Journal of Medical Genetics
Format: Online Article RSS Article
Published: 2026
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container_title Balkan Journal of Medical Genetics
description
discipline_display Medical Geneticsx
discipline_facet Medical Geneticsx
format Online Article
RSS Article
genre Journal Article
id rss_article:62497
institution FRELIP
journal_source_facet Balkan Journal of Medical Genetics
publishDate 2026
publishDateSort 2026
record_format rss_article
spellingShingle Townes–Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family
Medical Geneticsx
General
Medical Geneticsx
sub_discipline_display General
sub_discipline_facet General
subject_display Medical Geneticsx
General
Medical Geneticsx
Medical Geneticsx
General
Medical Geneticsx
subject_facet Medical Geneticsx
General
Medical Geneticsx
title Townes–Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family
title_auth Townes–Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family
title_full Townes–Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family
title_fullStr Townes–Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family
title_full_unstemmed Townes–Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family
title_short Townes–Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family
title_sort townes–brocks syndrome with consistent renal hypodysplasia and variable extrarenal features across three generations of serbian family
topic Medical Geneticsx
General
Medical Geneticsx
url https://sciendo.com/article/10.2478/bjmg-2025-00016