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Subject Item

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научни чланак 1981年の論文 1981年論文 vetenskaplig artikel 1981年論文 bài báo khoa học 1981年論文 artikulong pang-agham мақолаи илмӣ article scientific vitenskapelig artikkel vědecký článek articolo scientifico 1981 nî lūn-bûn научная статья bilimsel makale научни чланак 1981年论文 wetenschappelijk artikel scienca artikolo سائنسی مضمون מאמר מדעי article científic videnskabelig artikel (udgivet 1981) vedecký článok mokslinis straipsnis article scientifique (publié 1981) artykuł naukowy บทความทางวิทยาศาสตร์ 1981年论文 مقالهٔ علمی мақолаи илмӣ naučni članak artigo científico (publicado na 1981) artigo científico (publicado na 1981) 1981年論文 artikull shkencor 1981年论文 ১৯৮১-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ teaduslik artikkel научна статия 1981年论文 tieteellinen artikkeli artigo científico tudományos cikk 1981 թվականի մարտին հրատարակված գիտական հոդված επιστημονικό άρθρο 1981年論文 наукова стаття, опублікована в березні 1981 artículo científico publicado en 1981 scientific article articol științific 1981年论文 wissenschaftlicher Artikel artículu científicu espublizáu en 1981 مقالة علمية 1981年论文 1981년 논문 1981 թուականի Մարտին հրատարակուած գիտական յօդուած vitskapeleg artikkel სამეცნიერო სტატია

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1981-03-01T00:00:00Z

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J A Fleischman F E O'Donnell

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Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus

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Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus

schema:name

Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus

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Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus

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468-472

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n12:ARCHOPHT.1981.03930010470016

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10.1001/ARCHOPHT.1981.03930010470016