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Katja Dumic Kubat (@katjadumickubat) Instagram Profile Photo katjadumickubat. Katja Dumic Kubat. Krešimir Akrap (@kresoakrap) Instagram Profile Photo ...
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Researchgate: Katja Dumic
Zagreb, Croatia
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Clinical, Biochemical and Molecular Characteristics of the Patients...
abstracts.eurospe.org
Miroslav Dumica, Nevena Krnicb, Vesna Kusecc, Zorana Grubicd, Katarina Stingld, Tony Yuene, Katja Dumic Kubatb, Veselin Skrabicf & Maria I Newe.
Hydroxylase Deficiency - Ebscosearch.ebscohost.com › login › xoCFM+xSZk6
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Katja Dumic,1 Tony Yuen,2 Zorana Grubic,3 Vesna Kusec,4. Ingeborg Barisic,1 and Maria I. New2. 1 Division of Clinical Genetics, Department ...
Steroid 11-beta hydroxylase deficiency caused by compound ...search.proquest.com › openview › 1.pdf
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DS+4A to G) in one CYP11B1 allele and R448H in exon. 8 in the other. Katja Dumic & Robert Wilson & Pavinee Thanasawat &. Zorana Grubic ...
Publications
Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian...
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Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11β-Hydroxylase Deficiency. Katja Dumic,1 Tony Yuen,2 ...
Acknowledgement to Referees | SpringerLink
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Joe Dobosy, USA. Luciana Lara dos Santos, Brazil. Nick Dragojlovic, Canada. Katja Dumic, Croatia. David A. Dyment, Canada. Henry Ebili, UK.
Steroid 11-beta hydroxylase deficiency caused by compound...
link.springer.com
Katja Dumic (1) Robert Wilson (2) Pavinee Thanasawat (2) Zorana Grubic (3) Vesna Kusec (4) Katarina Stingl (3) Maria I. New (2) Author Affiliations. 1. Department of
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Katja Dumic Kubat | LinkedIn
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katja dumic | LinkedIn
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katja dumic Student at Sveuèilište u Zagrebu Location Croatia Industry Medical Practice Join LinkedIn and access katja dumic’s full profile. As a LinkedIn member ...
Clinical and Experimental Reproductive Medicine
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... 2Hypochondroplasia due to FGFR3 gene mutation (N540K) and mosaic form of Down syndrome in the same patient, Katja Dumic, Ingeborg Barisic, ...
Cureus | Two Novel CYP11B1 Gene Mutations in Patients from Two...
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Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11β-Hydroxylase Deficiency. Katja Dumic, Tony Yuen, Zorana Grubic, Vesna ...
Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian...
cyberleninka.org
Similar topics of scientific paper in Biological sciences , author of scholarly article — Katja Dumic, Tony Yuen, Zorana Grubic, Vesna Kusec, Ingeborg Barisic, ...
(PDF) Untreated congenital adrenal hyperplasia due to 21-hydroxylase...
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Untreated congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Two novel CYP11B1 gene mutations in patients from two Croatian...
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Gale OneFile includes Two novel CYP11B1 gene mutations in patients from two C by Katja Dumic, Tony Yuen, Zorana Grubic, . Click to explore.
achondroplasia - Labome.Org
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... D R Berk · Moise Danielpour · Paweł Koczewski · A Aviv · Anastasia Konstantinidou · George Georgoulis · Li Dai · Katja Dumic · Banu Cevik ...
Untreated congenital adrenal hyperplasia due to 21 hydroxylase...
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Discuss about this paper : Untreated congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Platform for researcher
Katja Dumić Kubat - pedijatar, iskustva pacijenata
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Katja Dumić Kubat, Grad Zagreb, Maksimir, KBC Zagreb - Rebro, Kišpatićeva 12, pedijatar - iskustva pacijenata: 1 ocjena, 10 komentara. Ako Vam je ovaj liječnik...
Više o temi Katja Dumić Kubat | Telegram.hr
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