"congenital malformation" trang 2 - tải miễn phí từ tailieunhanh
Ebook Fundamentals of congenital minimally invasive cardiac surgery: Part 1

Ebook Fundamentals of congenital minimally invasive cardiac surgery: Part 1
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Ebook Fundamentals of congenital minimally invasive cardiac surgery: Part 2

Ebook Fundamentals of congenital minimally invasive cardiac surgery: Part 2
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Whole exome sequencing revealed a mutation in COL6A1 associated with ullrich congenital muscular dystrophy

Whole exome sequencing revealed a mutation in COL6A1 associated with ullrich congenital muscular dystrophy
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Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: A case report

Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: A case report
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Abnormal Brain Development in Newborns with Congenital Heart Disease

Abnormal Brain Development in Newborns with Congenital Heart Disease
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Ebook Ultrasound of congenital fetal anomalies - Differential diagnosis and prognostic indicators (2nd edition): Part 2

Ebook Ultrasound of congenital fetal anomalies - Differential diagnosis and prognostic indicators (2nd edition): Part 2
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Ebook USMLE road map - Genetics: Part 2

Ebook USMLE road map - Genetics: Part 2
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Ebook Pediatric cardiology - The essential pocket guide (3rd edition): Part 2

Ebook Pediatric cardiology - The essential pocket guide (3rd edition): Part 2
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Ebook Moss & adams heart disease in infants, children, and adolescents: Part 2

Ebook Moss & adams heart disease in infants, children, and adolescents: Part 2
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Ebook Comprehensive surgical management of congenital heart disease (2/E): Part 2

Ebook Comprehensive surgical management of congenital heart disease (2/E): Part 2
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Impact on parents of bronchiolitis hospitalization of full-term, preterm and congenital heart disease infants

Impact on parents of bronchiolitis hospitalization of full-term, preterm and congenital heart disease infants
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Epidemiology of isolated preaxial polydactyly type I: Data from the Polish Registry of Congenital Malformations (PRCM)

Epidemiology of isolated preaxial polydactyly type I: Data from the Polish Registry of Congenital Malformations (PRCM)
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MEF2C loss-of-function mutation contributes to congenital heart defects

MEF2C loss-of-function mutation contributes to congenital heart defects
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Severe late-onset multisystem cytomegalovirus infection in a premature neonate previously treated for congenital infection

Severe late-onset multisystem cytomegalovirus infection in a premature neonate previously treated for congenital infection
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Hypoglycemia in patients with congenital muscle disease

Hypoglycemia in patients with congenital muscle disease
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Risk factors for low cardiac output syndrome in children with congenital heart disease undergoing cardiac surgery: A retrospective cohort study

Risk factors for low cardiac output syndrome in children with congenital heart disease undergoing cardiac surgery: A retrospective cohort study
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The VICI-trial: High frequency oscillation versus conventional mechanical ventilation in newborns with congenital diaphragmatic hernia: An international multicentre randomized controlled trial

The VICI-trial: High frequency oscillation versus conventional mechanical ventilation in newborns with congenital diaphragmatic hernia: An international multicentre randomized controlled trial
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The expression of Gli3 and Teashirt3 in the stenotic tissue of congenital pelvi ureteric junction obstruction in children

The expression of Gli3 and Teashirt3 in the stenotic tissue of congenital pelvi ureteric junction obstruction in children
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Investigation of somatic NKX2-5 mutations in Chinese children with congenital heart disease

Investigation of somatic NKX2-5 mutations in Chinese children with congenital heart disease
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Bài giảng Thông nối cửa chủ bẩm sinh Congenital Portosystemic Shunts – BS.CK2 Nguyễn Hữu Chí

Bài giảng Thông nối cửa chủ bẩm sinh Congenital Portosystemic Shunts – BS.CK2 Nguyễn Hữu Chí
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