"Autosomal recessive disorder" trang 1 - tải miễn phí từ tailieuXANH
Ebook USMLE road map - Genetics: Part 1

Ebook USMLE road map - Genetics: Part 1
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Báo cáo sinh học:

Báo cáo sinh học: "Phenotypic plasticity of body pigmentation in Drosophila: Autosomal recessive myotonia in sheep"
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Báo cáo sinh học:

Báo cáo sinh học: " Autosomal recessive myotonia in sheep"
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Báo cáo y học:

Báo cáo y học: "Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia"
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Báo cáo khoa học: Emerging pathways in genetic Parkinson’s disease: Autosomal-recessive genes in Parkinson’s disease – a common pathway?

Báo cáo khoa học: Emerging pathways in genetic Parkinson’s disease: Autosomal-recessive genes in Parkinson’s disease – a common pathway?
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Stable clinical course in three siblings with late-onset isolated sulfite oxidase deficiency: A case series and literature review

Stable clinical course in three siblings with late-onset isolated sulfite oxidase deficiency: A case series and literature review
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The mystery of persistent pulmonary hypertension: An idiopathic infantile arterial calcification

The mystery of persistent pulmonary hypertension: An idiopathic infantile arterial calcification
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Trientine induced colitis during therapy for Wilson disease: A case report and review of the literature

Trientine induced colitis during therapy for Wilson disease: A case report and review of the literature
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Phenylketonuria screening in Iranian newborns: A systematic review and metaanalysis

Phenylketonuria screening in Iranian newborns: A systematic review and metaanalysis
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CATCHing putative causative variants in consanguineous families

CATCHing putative causative variants in consanguineous families
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Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies

Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies
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Novel genetic variant of HPS1 gene in Hermansky-Pudlak syndrome with fulminant progression of pulmonary fibrosis: A case report

Novel genetic variant of HPS1 gene in Hermansky-Pudlak syndrome with fulminant progression of pulmonary fibrosis: A case report
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Anesthetic experience of an adult male with citrullinemia type II: A case report

Anesthetic experience of an adult male with citrullinemia type II: A case report
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A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs

A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs
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A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle

A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle
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Autosomal recessive loci contribute significantly to quantitative variation of male fertility in a dairy cattle population

Autosomal recessive loci contribute significantly to quantitative variation of male fertility in a dairy cattle population
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