A new form of total anomalous pulmonary venous connection with double drainage

スポンサーリンク

概要

論文の詳細を見る
2000-08-01

著者

関連論文

Genetic Analysis of Shwachman-Diamond Syndrome : Phenotypic Heterogeneity in Patients Carrying Identical SBDS Mutations
Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese
Mutation analysis of phenylketonuria in Yamagata prefecture, Japan
De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : unequal sister chromatid exchange during paternal gametogenesis
Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene : The common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese
Congenital Central Hypoventilation Syndrome : A Novel Mutation of the RET Gene in an Isolated Case
Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease
Successful Unrelated Donor Bone Marrow Transplantation for Shwachman-Diamond Syndrome with Leukemia
CD48 expression on leukocytes in infectious diseases: Flow cytometric analysis of surface antigen
Polymorphisms of Heme Oxygenase-1 and Bilirubin UDP-Glucuronosyltransferase Genes are not Associated with Kawasaki Disease Susceptibility
Contracted form of endocardial fibroelastosis in two siblings
A new form of total anomalous pulmonary venous connection with double drainage
Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease
Sudden Infant Death Syndrome Is Not Associated with the Mutation of PHOX2B Gene, a Major Causative Gene of Congenital Central Hypoventilation Syndrome
Beraprost sodium for pulmonary hypertension with congenital heart disease
Management of Functional Pulmonary Atresia with Isoproterenol in a Neonate with Ebstein's Anomaly
Microangiopathic Hemolytic Anemia and Thrombocytopenia in a Child with Atrial Septal Defect and Pulmonary Hypertension
Left and right ventricular volume characteristics in tetralogy of Fallot and their relationship to arterial oxygen saturation and age
Angiographic Determination of Left and Right Ventricular Volumes and Left Ventricular Mass in Normal Infants and Children
A case of progressive familial intrahepatic cholestasis type 1 with compound heterozygous mutations of ATP8B1
Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome
Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan
Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease : nonsense mutation probably causes a recessive phenotype
Polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : rs17884724:A>C is associated with 7-alanine expansion
Phenotypic variability in a family with Townes-Brocks syndrome
Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1

もっと見る

スポンサーリンク