Defects 22q11 deletion syndrome. Medical search. Frequent questions

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Anatomy7

Chromosomes, Human, Pair 22 Parietal Bone Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 6 Branchial Region Brain Chromosomes, Human, Pair 18

Organisms3

Staphylococcus lugdunensis Mice, Inbred C57BL Mice, Knockout

Diseases42

22q11 Deletion Syndrome DiGeorge Syndrome Syndrome Chromosome Deletion Velopharyngeal Insufficiency Abnormalities, Multiple Craniofacial Abnormalities Chromosome Disorders Intellectual Disability Jacobsen Distal 11q Deletion Syndrome Hypoparathyroidism Cri-du-Chat Syndrome Heart Defects, Congenital Facies Chromosome Breakage Hypocalcemia WAGR Syndrome Muscle Hypotonia Eye Abnormalities Exostoses, Multiple Hereditary Learning Disorders Down Syndrome Metabolic Syndrome X Monosomy Language Development Disorders Chromosome Aberrations Cleft Palate Nephrotic Syndrome Growth Disorders Sjogren's Syndrome Translocation, Genetic Seizures Turner Syndrome Genetic Predisposition to Disease Myelodysplastic Syndromes Williams Syndrome Prader-Willi Syndrome Heart Septal Defects, Ventricular Cushing Syndrome Polycystic Ovary Syndrome Acute Coronary Syndrome Heart Septal Defects, Atrial

Chemicals and Drugs3

Catechol O-Methyltransferase T-Box Domain Proteins Complement C1q

Analytical, Diagnostic and Therapeutic Techniques and Equipment13

In Situ Hybridization, Fluorescence Facies Karyotyping Pedigree Chromosome Mapping Comparative Genomic Hybridization Chromosome Banding Magnetic Resonance Imaging Case-Control Studies Genetic Association Studies DNA Mutational Analysis Analysis of Variance Polymerase Chain Reaction

Psychiatry and Psychology13

Intellectual Disability Developmental Disabilities Schizophrenia Stanford-Binet Test Learning Disorders Intelligence Tests Siblings Cognition Disorders Intelligence Neuropsychological Tests Psychotic Disorders Psychiatric Status Rating Scales Mental Disorders

Phenomena and Processes22

Chromosomes, Human, Pair 22 Chromosome Deletion Gene Deletion Sequence Deletion Phenotype Hemizygote Chromosome Breakage Mutation Monosomy Chromosome Aberrations Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 6 Base Sequence Genotype Gene Dosage Gene Rearrangement Translocation, Genetic Amino Acid Sequence Chromosomes, Human, Pair 18 Genetic Predisposition to Disease Polymorphism, Single Nucleotide Exons

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups2

Infant, Newborn Siblings

Health Care2

Case-Control Studies Analysis of Variance

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 Information Science Named Groups Health Care

22q11 Deletion Syndrome DiGeorge Syndrome Chromosomes, Human, Pair 22 Syndrome Chromosome Deletion Velopharyngeal Insufficiency Gene Deletion Abnormalities, Multiple Craniofacial Abnormalities Chromosome Disorders Sequence Deletion Intellectual Disability Jacobsen Distal 11q Deletion Syndrome Hypoparathyroidism Phenotype Developmental Disabilities Parietal Bone Cri-du-Chat Syndrome Hemizygote In Situ Hybridization, Fluorescence Heart Defects, Congenital Facies Chromosome Breakage Hypocalcemia Catechol O-Methyltransferase WAGR Syndrome Karyotyping Mutation Muscle Hypotonia Eye Abnormalities Schizophrenia T-Box Domain Proteins Stanford-Binet Test Molecular Sequence Data Exostoses, Multiple Hereditary Learning Disorders Down Syndrome Metabolic Syndrome X Pedigree Monosomy Language Development Disorders Chromosome Mapping Comparative Genomic Hybridization Chromosome Aberrations Chromosome Banding Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 6 Staphylococcus lugdunensis Cleft Palate Base Sequence Branchial Region Infant, Newborn Genotype Intelligence Tests Brain Gene Dosage Magnetic Resonance Imaging Nephrotic Syndrome Siblings Growth Disorders Gene Rearrangement Sjogren's Syndrome Case-Control Studies Translocation, Genetic Cognition Disorders Amino Acid Sequence Chromosomes, Human, Pair 18 Intelligence Neuropsychological Tests Seizures Genetic Association Studies Turner Syndrome Psychotic Disorders Mice, Inbred C57BL Psychiatric Status Rating Scales Genetic Predisposition to Disease Myelodysplastic Syndromes Williams Syndrome Complement C1q DNA Mutational Analysis Polymorphism, Single Nucleotide Prader-Willi Syndrome Heart Septal Defects, Ventricular Analysis of Variance Cushing Syndrome Mental Disorders Mice, Knockout Polycystic Ovary Syndrome Acute Coronary Syndrome Heart Septal Defects, Atrial Polymerase Chain Reaction Exons

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