"inherited disorders" trang 2 - tải miễn phí từ tailieuXANH
Ebook Clinical arrhythmology: Part 2

Ebook Clinical arrhythmology: Part 2
251    41    0
Ebook Heart rate and rhythm molecular basis pharmacological modulation and clinical implications: Part 2

Ebook Heart rate and rhythm molecular basis pharmacological modulation and clinical implications: Part 2
294    55    0
Ebook Lecture notes dermatology (11th edition): Part 2

Ebook Lecture notes dermatology (11th edition): Part 2
115    57    0
Object Oriented Programming - Lesson 6: Inheritance

Object Oriented Programming - Lesson 6: Inheritance
34    51    0
Ebook Cambridge international AS and A level - Biology coursebook: Part 2

Ebook Cambridge international AS and A level - Biology coursebook: Part 2
401    64    3
Bài giảng môn Lập trình hướng đối tượng: Chương 11 - TS. Nguyễn Văn Hiệp

Bài giảng môn Lập trình hướng đối tượng: Chương 11 - TS. Nguyễn Văn Hiệp
42    34    0
Ebook Oxford textbook of neuromuscular disorders: Part 2

Ebook Oxford textbook of neuromuscular disorders: Part 2
210    43    0
Ebook Practical nephrology: Part 2

Ebook Practical nephrology: Part 2
467    47    0
Genetic differentiation and polyploid formation within the Cryptogramma crispa complex (Polypodiales: Pteridaceae)

Genetic differentiation and polyploid formation within the Cryptogramma crispa complex (Polypodiales: Pteridaceae)
10    52    0
Allogeneic hematopoietic stem cell transplantation for non-malignant hematological disorders

Allogeneic hematopoietic stem cell transplantation for non-malignant hematological disorders
10    48    0
Management of dystocia in buffalo due to Dicephalus Ischiopagus Tetrabrachius tetrapus monster calf

Management of dystocia in buffalo due to Dicephalus Ischiopagus Tetrabrachius tetrapus monster calf
3    50    0
Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutarylCoA synthase deficiency associated with two novel mutations: A case report

Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutarylCoA synthase deficiency associated with two novel mutations: A case report
6    39    0
A heterozygous variant in the SLC22A12 gene in a Sri Lanka family associated with mild renal hypouricemia

A heterozygous variant in the SLC22A12 gene in a Sri Lanka family associated with mild renal hypouricemia
5    53    0
Application of protection motivation theory to clinical trial enrolment for pediatric chronic conditions

Application of protection motivation theory to clinical trial enrolment for pediatric chronic conditions
14    47    0
Nitrogen-fixing bacteria and Oxalis – evidence for a vertically inherited bacterial symbiosis

Nitrogen-fixing bacteria and Oxalis – evidence for a vertically inherited bacterial symbiosis
10    67    0
High-resolution mapping and characterization of qRgls2, a major quantitative trait locus involved in maize resistance to gray leaf spot

High-resolution mapping and characterization of qRgls2, a major quantitative trait locus involved in maize resistance to gray leaf spot
10    63    0
Potential genetic modifiers for somatic EGFR mutation in lung cancer: A metaanalysis and literature review

Potential genetic modifiers for somatic EGFR mutation in lung cancer: A metaanalysis and literature review
17    122    0
Evaluation for inherited and acquired prothrombotic defects predisposing to symptomatic thromboembolism in children with acute lymphoblastic leukemia: A protocol for a prospective, observational, cohort study

Evaluation for inherited and acquired prothrombotic defects predisposing to symptomatic thromboembolism in children with acute lymphoblastic leukemia: A protocol for a prospective, observational, cohort study
14    62    0
A novel deleterious PTEN mutation in a patient with early-onset bilateral breast cancer

A novel deleterious PTEN mutation in a patient with early-onset bilateral breast cancer
6    95    0
Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes

Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes
6    55    0
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