Constitutional isomerism. Medical search. Frequent questions

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Anatomy32

Heart Atria Venae Cavae Chromosomes, Human, Pair 22 Pulmonary Veins Chromosomes, Human, Pair 11 Fetal Heart Atrioventricular Node Vena Cava, Inferior Azygos Vein Ring Chromosomes Sinoatrial Node Heart Valves Atrial Appendage Chromosomes, Human, 21-22 and Y Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 3 Hybrid Cells Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 9 Spleen Chromosomes, Human Chromosomes, Human, Pair 12 Stomach Telomere Lymphocytes X Chromosome Spermatozoa Bone Marrow Cell Line

Organisms1

Diseases56

Heterotaxy Syndrome Heart Defects, Congenital Puberty, Delayed Abnormalities, Multiple Situs Inversus Heart Septal Defects Dextrocardia Levocardia Pulmonary Veno-Occlusive Disease Cyanosis Coxa Vara Wilms Tumor Growth Disorders Translocation, Genetic Syndrome Neurofibromatosis 2 Chromosome Breakage Fetal Diseases Chromosome Deletion Primary Myelofibrosis Ring Chromosomes Tachycardia, Supraventricular Heart Block Neurofibromatoses Chromosome Aberrations Heart Septal Defects, Atrial Chromosome Disorders Beckwith-Wiedemann Syndrome Retinoblastoma Sunburn Li-Fraumeni Syndrome Kidney Neoplasms Myxoma Intellectual Disability Aneuploidy Neuronal Migration Disorders Genetic Predisposition to Disease Chromosome Fragility DiGeorge Syndrome Neurofibromatosis 1 Sex Chromosome Aberrations Splenomegaly Chromosome Inversion Skin Neoplasms Heart Neoplasms Neoplasms Colorectal Neoplasms, Hereditary Nonpolyposis Carcinoma, Renal Cell Neoplasms, Multiple Primary Melanoma Adenomatous Polyposis Coli Leukemia Breast Neoplasms Ovarian Neoplasms Recurrence Disease Progression

Chemicals and Drugs25

Oxandrolone Erythrocruorins Growth Differentiation Factor 1 Nodal Protein Proline DNA, Neoplasm Neurofibromin 2 WT1 Proteins Genetic Markers DNA Probes Ghrelin DNA, Satellite DNA Janus Kinase 2 DNA-Binding Proteins Nuclear Proteins Adaptor Proteins, Signal Transducing Interferon-alpha Testosterone Adrenal Cortex Hormones Recombinant Proteins Transcription Factors DNA Primers Neoplasm Proteins Antineoplastic Agents

Analytical, Diagnostic and Therapeutic Techniques and Equipment50

Heart Bypass, Right Abortion, Eugenic Medicine, Korean Traditional Fontan Procedure In Situ Hybridization, Fluorescence Karyotyping Body Constitution Ultrasonography, Prenatal Pedigree Somatotypes Age Determination by Skeleton Magnetic Resonance Spectroscopy Prenatal Diagnosis Skin Pigmentation Chromosome Mapping DNA Mutational Analysis Chromosome Banding Retrospective Studies Body Height Echocardiography Treatment Outcome Follow-Up Studies Physical Chromosome Mapping Comparative Genomic Hybridization Polymerase Chain Reaction Models, Molecular Sequence Analysis, DNA Genetic Testing Blotting, Southern Drug Evaluation Anthropometry Nucleic Acid Hybridization Fatal Outcome Case-Control Studies Risk Factors Cohort Studies Drug Administration Schedule Oligonucleotide Array Sequence Analysis Prognosis Pilot Projects Antineoplastic Combined Chemotherapy Protocols Models, Genetic Reverse Transcriptase Polymerase Chain Reaction Incidence Risk Assessment Prospective Studies Survival Analysis Survival Rate Severity of Illness Index Immunohistochemistry

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes72

Isomerism Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 11 AT Rich Sequence Mosaicism Translocation, Genetic Chromosome Breakage Chromosome Deletion Ring Chromosomes Body Constitution Germ-Line Mutation Genes, Neurofibromatosis 1 Chromosome Aberrations Heterozygote Pregnancy Chromosomes, Human, 21-22 and Y Somatotypes Chromosomes, Human, Pair 17 Skin Pigmentation Body Patterning Chromosomes, Human, Pair 5 Stereoisomerism Mutation Alleles Genes, Wilms Tumor Body Height Aneuploidy Chromosomes, Human, Pair 1 Genetic Predisposition to Disease Chromosomes, Human, Pair 13 Gene Deletion Sunlight Chromosome Fragility Gestational Age Loss of Heterozygosity Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 9 Sex Chromosome Aberrations Phenotype Molecular Structure Genetic Markers Gene Rearrangement Chromosome Inversion Puberty Chromosomes, Human Base Sequence Genome, Human Chromosomes, Human, Pair 12 Time Factors Polymorphism, Genetic Polymorphism, Restriction Fragment Length Genes, Tumor Suppressor Genotype Protein Conformation DNA, Satellite Exons Telomere Gene Dosage Nucleic Acid Hybridization DNA Methylation Genetic Linkage Haplotypes Mutation, Missense Microsatellite Repeats Homozygote X Chromosome Point Mutation Genes, p53 Repetitive Sequences, Nucleic Acid Sequence Deletion Polymorphism, Single Nucleotide

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena6

Supreme Court Decisions Civil Rights Medicine, Korean Traditional Democracy Government Regulation Family

Humanities1

Awards and Prizes

Information Science5

Molecular Sequence Data Base Sequence Fatal Outcome Incidence Survival Rate

Named Groups2

Persons Infant, Newborn

Health Care22

Civil Rights Retrospective Studies Treatment Outcome Government Regulation Sunlight Follow-Up Studies Genetic Testing Family Health Anthropometry Fatal Outcome Case-Control Studies Risk Factors Cohort Studies Age Factors Pilot Projects Sex Factors Incidence Risk Assessment Prospective Studies Survival Analysis Survival Rate Severity of Illness Index

Geographicals2

Asia United States

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Anthropology, Education, Sociology and Social Phenomena Humanities Information Science Named Groups Health Care Geographicals

Isomerism Heterotaxy Syndrome Heart Defects, Congenital Puberty, Delayed Heart Atria Abnormalities, Multiple Situs Inversus Heart Septal Defects Venae Cavae Dextrocardia Levocardia Heart Bypass, Right Chromosomes, Human, Pair 22 Oxandrolone Pulmonary Veins Erythrocruorins Pulmonary Veno-Occlusive Disease Supreme Court Decisions Chromosomes, Human, Pair 11 AT Rich Sequence Mosaicism Growth Differentiation Factor 1 Fetal Heart Cyanosis Coxa Vara Abortion, Eugenic Wilms Tumor Growth Disorders Civil Rights Translocation, Genetic Medicine, Korean Traditional Syndrome Nodal Protein Atrioventricular Node Neurofibromatosis 2 Chromosome Breakage Fetal Diseases Vena Cava, Inferior Persons Chromosome Deletion Primary Myelofibrosis Fontan Procedure Azygos Vein Ring Chromosomes In Situ Hybridization, Fluorescence Karyotyping Tachycardia, Supraventricular Sinoatrial Node Infant, Newborn Body Constitution Heart Block Germ-Line Mutation Neurofibromatoses Genes, Neurofibromatosis 1 Chromosome Aberrations Ultrasonography, Prenatal Democracy Heterozygote Heart Valves Pedigree Atrial Appendage Pregnancy Chromosomes, Human, 21-22 and Y Somatotypes Heart Septal Defects, Atrial Age Determination by Skeleton Magnetic Resonance Spectroscopy Proline Chromosome Disorders Prenatal Diagnosis Chromosomes, Human, Pair 17 Beckwith-Wiedemann Syndrome Retinoblastoma Skin Pigmentation Chromosome Mapping Sunburn Li-Fraumeni Syndrome Kidney Neoplasms Body Patterning DNA Mutational Analysis Chromosome Banding Chromosomes, Human, Pair 5 Stereoisomerism Mutation Alleles Genes, Wilms Tumor Retrospective Studies Body Height Myxoma Echocardiography Epimedium Treatment Outcome Intellectual Disability Aneuploidy Neuronal Migration Disorders DNA, Neoplasm Chromosomes, Human, Pair 1 Genetic Predisposition to Disease Government Regulation Chromosomes, Human, Pair 13

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