Congenital heart defects digeorge syndrome. Medical search. Frequent questions

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Anatomy12

Chromosomes, Human, Pair 22 Heart Fetal Heart Branchial Region Neural Crest Thymus Gland Heart Valves Parathyroid Glands Embryo, Mammalian Aorta, Thoracic Pulmonary Artery Face

Diseases39

DiGeorge Syndrome Heart Defects, Congenital Abnormalities, Multiple Syndrome Cardiovascular Abnormalities Truncus Arteriosus, Persistent Chromosome Deletion Heart Septal Defects, Ventricular Down Syndrome Heart Septal Defects Cyanosis Hypocalcemia Heart Septal Defects, Atrial Endocardial Cushion Defects Hypoparathyroidism Tetralogy of Fallot Noonan Syndrome Immunologic Deficiency Syndromes Monosomy Hypoplastic Left Heart Syndrome Transposition of Great Vessels Facies Fetal Diseases Heart Diseases Musculoskeletal Abnormalities Chromosome Aberrations Tricuspid Atresia Situs Inversus Pulmonary Valve Stenosis Wolf-Hirschhorn Syndrome Intellectual Disability Ductus Arteriosus, Patent Heart Block Trisomy Translocation, Genetic Chromosome Disorders Heart Failure Craniofacial Abnormalities Aortic Coarctation

Chemicals and Drugs3

T-Box Domain Proteins Histone Chaperones Growth Differentiation Factor 1

Analytical, Diagnostic and Therapeutic Techniques and Equipment19

In Situ Hybridization, Fluorescence Ultrasonography, Prenatal Cardiac Surgical Procedures Heart Rate Facies Neonatal Screening Echocardiography Oximetry Retrospective Studies Prenatal Diagnosis Karyotyping Nuchal Translucency Measurement In Situ Hybridization Echocardiography, Four-Dimensional Chromosome Mapping Case-Control Studies Risk Factors Prospective Studies Pedigree

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes14

Chromosomes, Human, Pair 22 Chromosome Deletion Pregnancy Phenotype Heart Rate Gene Deletion Monosomy Gene Expression Regulation, Developmental Mutation Gestational Age Chromosome Aberrations Trisomy Translocation, Genetic Base Sequence

Information Science2

Molecular Sequence Data Base Sequence

Named Groups1

Infant, Newborn

Health Care5

Neonatal Screening Retrospective Studies Case-Control Studies Risk Factors Prospective Studies

Geographicals1

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Named Groups Health Care Geographicals

DiGeorge Syndrome Heart Defects, Congenital Chromosomes, Human, Pair 22 Abnormalities, Multiple Syndrome Cardiovascular Abnormalities T-Box Domain Proteins Heart Truncus Arteriosus, Persistent Chromosome Deletion Infant, Newborn Fetal Heart Heart Septal Defects, Ventricular Branchial Region Down Syndrome Heart Septal Defects Cyanosis Hypocalcemia Histone Chaperones Heart Septal Defects, Atrial In Situ Hybridization, Fluorescence Endocardial Cushion Defects Pregnancy Ultrasonography, Prenatal Hypoparathyroidism Phenotype Tetralogy of Fallot Growth Differentiation Factor 1 Noonan Syndrome Cardiac Surgical Procedures Neural Crest Immunologic Deficiency Syndromes Heart Rate Gene Deletion Monosomy Thymus Gland Gene Expression Regulation, Developmental Heart Valves Hypoplastic Left Heart Syndrome Transposition of Great Vessels Facies Neonatal Screening Mutation Parathyroid Glands Echocardiography Fetal Diseases Gestational Age Heart Diseases Oximetry Arkansas Musculoskeletal Abnormalities Chromosome Aberrations Tricuspid Atresia Embryo, Mammalian Retrospective Studies Molecular Sequence Data Prenatal Diagnosis Karyotyping Nuchal Translucency Measurement In Situ Hybridization Situs Inversus Aorta, Thoracic Pulmonary Valve Stenosis Echocardiography, Four-Dimensional Wolf-Hirschhorn Syndrome Intellectual Disability Chromosome Mapping Ductus Arteriosus, Patent Heart Block Pulmonary Artery Case-Control Studies Trisomy Translocation, Genetic Risk Factors Chromosome Disorders Heart Failure Prospective Studies Craniofacial Abnormalities Pedigree Face Base Sequence Aortic Coarctation

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