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научни чланак vedecký článok мақолаи илмӣ vědecký článek научни чланак scienca artikolo artikulong pang-agham article scientifique scientific article published on 20 November 2014 videnskabelig artikel 2014年学术文章 2014年学术文章 наукова стаття, опублікована в листопаді 2014 επιστημονικό άρθρο article scientific vitskapeleg artikkel tieteellinen artikkeli wetenschappelijk artikel naučni članak 2014年學術文章 teaduslik artikkel bilimsel makale ২০ নভেম্বর ২০১৪-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ articolo scientifico 2014年學術文章 scientific article published on 20 November 2014 מאמר מדעי مقالة علمية نشرت في 20 نوفمبر 2014 vetenskaplig artikel 2014年學術文章 2014年の論文 scientific article published on 20 November 2014 artikel ilmiah научна статия artigo científico tudományos cikk 2014年学术文章 artigo científico articol științific 2014년 논문 2014 nî lūn-bûn 2014年學術文章 2014年學術文章 บทความทางวิทยาศาสตร์ wissenschaftlicher Artikel artikull shkencor bài báo khoa học 2014年学术文章 2014年学术文章 artículo científico publicado en 2014 artículu científicu სამეცნიერო სტატია 2014年学术文章 artykuł naukowy научная статья artigo científico vitenskapelig artikkel article científic
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Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
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Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
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Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
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Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
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