Genetic abnormalities congenital abnormalities. Medical search. Frequent questions

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Anatomy15

Chromosomes, Human, 6-12 and X Chromosomes, Human, Pair 17 Fetus Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 1 Chromosomes, Human Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 7 Brain Tumor Cells, Cultured

Organisms4

Mice, Knockout Mice, Transgenic Mice, Mutant Strains Mice, Inbred C57BL

Diseases56

Congenital Abnormalities Abnormalities, Multiple Chromosome Aberrations Abnormalities, Drug-Induced Arthrogryposis Hydranencephaly Chromosome Disorders Arbovirus Infections Fanconi Anemia Urogenital Abnormalities Translocation, Genetic Limb Deformities, Congenital Crisscross Heart Pregnancy Complications Cryptorchidism Heart Defects, Congenital Syndrome Intellectual Disability Fetal Diseases Fetal Death Abortion, Spontaneous Hypospadias Abnormal Karyotype Sex Chromosome Aberrations Trisomy Chromosome Deletion Aneuploidy Glucosephosphate Dehydrogenase Deficiency Birth Weight Multiple Myeloma Eye Abnormalities Leukemia, Myeloid, Acute Infertility, Male Myelodysplastic Syndromes Precursor Cell Lymphoblastic Leukemia-Lymphoma Oligospermia Lymphoma, Large B-Cell, Diffuse Leukemia, Lymphocytic, Chronic, B-Cell Disease Progression Genetic Predisposition to Disease Disease Models, Animal Precancerous Conditions Cell Transformation, Neoplastic Cardiovascular Abnormalities Craniofacial Abnormalities Lung Neoplasms Skin Abnormalities Neoplasms Brain Neoplasms Musculoskeletal Abnormalities Recurrence Tooth Abnormalities Adenocarcinoma Breast Neoplasms Brain Diseases Nervous System Malformations

Chemicals and Drugs19

Fanconi Anemia Complementation Group Proteins Teratogens 6-Mercaptopurine Sulfasalazine Azathioprine Oncogene Proteins, Fusion DNA, Neoplasm Core Binding Factor Alpha 2 Subunit Neoplasm Proteins Tumor Suppressor Protein p53 Tumor Markers, Biological Cyclin-Dependent Kinase Inhibitor p16 DNA-Binding Proteins Proto-Oncogene Proteins Genetic Markers RNA, Messenger Nuclear Proteins Antineoplastic Agents Transcription Factors

Analytical, Diagnostic and Therapeutic Techniques and Equipment46

Karyotyping In Situ Hybridization, Fluorescence Dermatoglyphics Pregnancy Outcome Perinatal Care Pedigree Preconception Care Prenatal Diagnosis Ultrasonography, Prenatal Risk Factors Retrospective Studies Cytogenetic Analysis Magnetic Resonance Imaging Case-Control Studies Infant Mortality Tomography, X-Ray Computed Comparative Genomic Hybridization Incidence Prognosis DNA Mutational Analysis Treatment Outcome Birth Weight Cohort Studies Genetic Testing Prospective Studies Polymerase Chain Reaction Immunohistochemistry Disease Models, Animal Gene Expression Profiling Nucleic Acid Hybridization Oligonucleotide Array Sequence Analysis Immunophenotyping Chromosome Mapping Reverse Transcriptase Polymerase Chain Reaction Blotting, Southern Neoplasm Staging Survival Analysis Flow Cytometry Electrocardiography Sensitivity and Specificity Chromosome Banding Follow-Up Studies Echocardiography Reference Values Biopsy Predictive Value of Tests

Psychiatry and Psychology2

Intellectual Disability Schizophrenia

Phenomena and Processes59

Chromosome Aberrations Pregnancy Translocation, Genetic Pregnancy Outcome Gestational Age Stillbirth Chromosomes, Human, 6-12 and X Phenotype Mutation Abnormal Karyotype Pregnancy Trimester, First Loss of Heterozygosity Sex Chromosome Aberrations Trisomy Chromosomes, Human, Pair 17 Chromosome Deletion Maternal Age Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 14 Genes, p53 Chromosomes, Human, Pair 9 Aneuploidy Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 1 Gene Deletion Chromosomes, Human Birth Weight Gene Rearrangement Chromosomes, Human, Pair 8 Ploidies Chromosomes, Human, Pair 7 Heterozygote Homozygote Gene Amplification Genetic Predisposition to Disease Polymorphism, Single-Stranded Conformational Genes, Tumor Suppressor Nucleic Acid Hybridization Microsatellite Repeats Base Sequence Gene Dosage Gene Expression Regulation, Neoplastic Oncogenes Genes, ras Genotype Exons Genetic Markers Point Mutation Alleles Apoptosis Gene Expression Signal Transduction Time Factors Polymorphism, Genetic Polymorphism, Single Nucleotide Drug Resistance, Neoplasm Sensitivity and Specificity

Disciplines and Occupations2

Immunohistochemistry Cytogenetics

Anthropology, Education, Sociology and Social Phenomena1

Dermatoglyphics

Information Science5

Infant Mortality Incidence Base Sequence Molecular Sequence Data Image Processing, Computer-Assisted

Named Groups2

Infant, Newborn Infant, Premature

Health Care17

Paternal Exposure Perinatal Care Preconception Care Risk Factors Maternal Age Retrospective Studies Case-Control Studies Infant Mortality Incidence Treatment Outcome Cohort Studies Genetic Testing Prospective Studies Survival Analysis Sensitivity and Specificity Follow-Up Studies Predictive Value of Tests

Geographicals4

Hungary Oman Denmark England

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

Congenital Abnormalities Abnormalities, Multiple Chromosome Aberrations Hungary Abnormalities, Drug-Induced Arthrogryposis Hydranencephaly Infant, Newborn Pregnancy Karyotyping Chromosome Disorders Arbovirus Infections Fanconi Anemia Urogenital Abnormalities Translocation, Genetic Limb Deformities, Congenital Crisscross Heart Pregnancy Complications Fanconi Anemia Complementation Group Proteins In Situ Hybridization, Fluorescence Cryptorchidism Heart Defects, Congenital Syndrome Dermatoglyphics Intellectual Disability Fetal Diseases Paternal Exposure Pregnancy Outcome Fetal Death Gestational Age Abortion, Spontaneous Stillbirth Perinatal Care Pedigree Chromosomes, Human, 6-12 and X Hypospadias Teratogens Phenotype Mutation 6-Mercaptopurine Preconception Care Prenatal Diagnosis Ultrasonography, Prenatal Abnormal Karyotype Pregnancy Trimester, First Loss of Heterozygosity Sex Chromosome Aberrations Trisomy Chromosomes, Human, Pair 17 Sulfasalazine Oman Chromosome Deletion Risk Factors Maternal Age Azathioprine Retrospective Studies Cytogenetic Analysis Magnetic Resonance Imaging Fetus Case-Control Studies Infant Mortality Chromosomes, Human, Pair 11 Denmark Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 14 Genes, p53 Tomography, X-Ray Computed Comparative Genomic Hybridization Incidence Chromosomes, Human, Pair 9 Infant, Premature Prognosis Oncogene Proteins, Fusion Aneuploidy Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 1 Gene Deletion DNA Mutational Analysis Treatment Outcome Chromosomes, Human Glucosephosphate Dehydrogenase Deficiency Birth Weight Gene Rearrangement Cohort Studies Chromosomes, Human, Pair 8 Genetic Testing Multiple Myeloma Eye Abnormalities Ploidies Leukemia, Myeloid, Acute DNA, Neoplasm Infertility, Male Prospective Studies Chromosomes, Human, Pair 7 Polymerase Chain Reaction Myelodysplastic Syndromes Heterozygote Precursor Cell Lymphoblastic Leukemia-Lymphoma England

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