Retardation occurs growth. Medical search. Frequent questions

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Anatomy37

Chromosomes, Human, X X Chromosome Face Brain Ring Chromosomes Facial Bones Placenta Chromosomes, Human, 6-12 and X Chromosomes, Human, Pair 15 Neurons Cell Line Toes Chromosomes, Human, 1-3 Fetus Chromosomes, Human, Pair 21 Growth Plate Chromosomes, Human, 13-15 Embryo, Mammalian Skull Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 4 Dendritic Spines Chromosomes, Human, Pair 8 Cells, Cultured Telomere Dendrites Chromosomes, Human, 4-5 Fibroblasts Chromosomes, Human, Pair 22 Hippocampus Chromosomes, Human, Pair 16 HeLa Cells Arm Bones Hair Bone and Bones Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 7

Organisms5

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

Diseases100

Intellectual Disability Mental Retardation, X-Linked Fetal Growth Retardation Fragile X Syndrome Abnormalities, Multiple Growth Disorders Syndrome Microcephaly Facies Psychomotor Disorders Sex Chromosome Aberrations Chromosome Deletion Muscle Hypotonia Ataxia Chromosome Disorders Chromosome Aberrations Trisomy Craniofacial Abnormalities Spasms, Infantile Failure to Thrive Rett Syndrome Dwarfism Fetal Death Hypertelorism Coloboma Ring Chromosomes Down Syndrome Epilepsy Hand Deformities, Congenital Monosomy Nervous System Malformations Abnormalities, Drug-Induced alpha-Thalassemia Translocation, Genetic Birth Weight Rubinstein-Taybi Syndrome Disease Models, Animal Seizures Bone Diseases, Developmental Fetal Weight Oculocerebrorenal Syndrome De Lange Syndrome Genetic Diseases, X-Linked Eye Abnormalities Ichthyosis Pregnancy Complications Foot Deformities, Congenital Congenital Abnormalities Agenesis of Corpus Callosum Cerebellar Ataxia Phenylketonurias Chromosome Breakage Congenital Hypothyroidism Tuberous Sclerosis Body Weight Angelman Syndrome Sex Chromosome Disorders Chromosome Fragility Wolf-Hirschhorn Syndrome Learning Disorders Classical Lissencephalies and Subcortical Band Heterotopias Fetal Diseases Carbohydrate Metabolism, Inborn Errors Language Development Disorders Coffin-Lowry Syndrome Smith-Lemli-Opitz Syndrome Fetal Alcohol Spectrum Disorders Blepharophimosis Cri-du-Chat Syndrome Nutrition Disorders Sjogren-Larsson Syndrome Skin Abnormalities WAGR Syndrome Chromosome Inversion Metabolism, Inborn Errors Heart Defects, Congenital Micrognathism Amino Acid Metabolism, Inborn Errors Embryo Loss Lissencephaly Syndactyly Tooth Abnormalities Prenatal Exposure Delayed Effects Prader-Willi Syndrome Tremor Microphthalmos Genetic Diseases, Inborn Heredodegenerative Disorders, Nervous System Williams Syndrome Hydrocephalus Cerebral Palsy Musculoskeletal Abnormalities Cleft Palate Osteochondrodysplasias Methemoglobinemia Urogenital Abnormalities Blepharoptosis Phenylketonuria, Maternal Pigmentation Disorders Nervous System Diseases

Chemicals and Drugs29

Fragile X Mental Retardation Protein RNA-Binding Proteins DNA-Binding Proteins Methyl-CpG-Binding Protein 2 Nuclear Proteins Transcription Factors RNA, Messenger Nerve Tissue Proteins DNA Hemoglobin H Repressor Proteins Codon, Nonsense Interleukin-1 Receptor Accessory Protein DNA Primers Genetic Markers Deoxyribonuclease I Receptors, Metabotropic Glutamate DNA Helicases Teratogens Adaptor Protein Complex sigma Subunits Growth Hormone Carrier Proteins Adenylosuccinate Lyase Methoxyhydroxyphenylglycol Receptor, Metabotropic Glutamate 5 Drosophila Proteins RNA Proteins Insulin-Like Growth Factor I

Analytical, Diagnostic and Therapeutic Techniques and Equipment27

Pedigree Facies Karyotyping In Situ Hybridization, Fluorescence Chromosome Banding Chromosome Mapping DNA Mutational Analysis Birth Weight Microscopy, Polarization Disease Models, Animal Body Height Fetal Weight Heterozygote Detection Body Weight Prenatal Diagnosis Genetic Testing Age Determination by Skeleton Comparative Genomic Hybridization Gene Targeting Dermatoglyphics Organ Size Polymerase Chain Reaction Transfection Cloning, Molecular Cordocentesis Pregnancy Outcome Restriction Mapping

Psychiatry and Psychology9

Intellectual Disability Psychomotor Disorders Developmental Disabilities Education of Intellectually Disabled Autistic Disorder Intelligence Tests Intelligence Learning Disorders Projective Techniques

Phenomena and Processes82

Sex Chromosome Aberrations Chromosomes, Human, X X Chromosome Base Sequence Pregnancy Birefringence Phenotype Mutation Consanguinity Chromosome Deletion Genes, Recessive Chromosome Aberrations Trisomy Growth Genetic Linkage Promoter Regions, Genetic Ring Chromosomes Amino Acid Sequence Heterozygote Gestational Age Embryonic and Fetal Development Monosomy Translocation, Genetic Gene Deletion Birth Weight Homozygote Body Height Transcription, Genetic Chromosomes, Human, 6-12 and X Fetal Weight Protein Binding Mosaicism Binding Sites Chromosomes, Human, Pair 15 Sequence Deletion Mutation, Missense Codon, Nonsense Trinucleotide Repeat Expansion Gene Expression Regulation Dosage Compensation, Genetic Chromosome Breakage Body Weight Gene Duplication Chromosome Fragility Exons Gene Expression Regulation, Developmental Genetic Markers Chromosomes, Human, 1-3 Chromosomes, Human, Pair 21 Gene Dosage Chromosomes, Human, 13-15 Fetal Development Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 4 Organ Size Chromosomes, Human, Pair 8 Telomere Transfection Regulatory Sequences, Nucleic Acid Chromosome Inversion Gene Expression Chromosomes, Human, 4-5 Maternal-Fetal Exchange Genotype Time Factors Protein Biosynthesis Alleles Pregnancy Outcome Genomic Imprinting Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 16 Frameshift Mutation Trinucleotide Repeats Plasmids Bone Development Embryonic Development Sequence Homology, Amino Acid X Chromosome Inactivation Genes, X-Linked Chromosome Fragile Sites Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 7

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Education of Intellectually Disabled Dermatoglyphics

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups3

Infant, Newborn Infant, Small for Gestational Age Infant, Low Birth Weight

Health Care3

Genetic Testing Group Homes Genetic Counseling

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

Intellectual Disability Mental Retardation, X-Linked Fragile X Mental Retardation Protein Fetal Growth Retardation Fragile X Syndrome Abnormalities, Multiple Growth Disorders Syndrome Microcephaly Pedigree Facies Psychomotor Disorders Sex Chromosome Aberrations Molecular Sequence Data Chromosomes, Human, X X Chromosome Base Sequence Pregnancy Birefringence Phenotype Mutation Consanguinity Developmental Disabilities Infant, Newborn Chromosome Deletion Muscle Hypotonia Karyotyping Ataxia Chromosome Disorders Genes, Recessive In Situ Hybridization, Fluorescence Education of Intellectually Disabled Chromosome Aberrations Trisomy RNA-Binding Proteins Chromosome Banding Growth DNA-Binding Proteins Genetic Linkage Craniofacial Abnormalities Spasms, Infantile Methyl-CpG-Binding Protein 2 Face Failure to Thrive Rett Syndrome Chromosome Mapping Dwarfism Mice, Knockout Fetal Death Autistic Disorder Nuclear Proteins Promoter Regions, Genetic Transcription Factors Brain Hypertelorism Coloboma Ring Chromosomes DNA Mutational Analysis Down Syndrome Epilepsy Amino Acid Sequence Heterozygote Hand Deformities, Congenital Gestational Age RNA, Messenger Facial Bones Nerve Tissue Proteins DNA Embryonic and Fetal Development Monosomy Nervous System Malformations Abnormalities, Drug-Induced alpha-Thalassemia Translocation, Genetic Gene Deletion Intelligence Tests Birth Weight Hemoglobin H Homozygote Rubinstein-Taybi Syndrome Placenta Microscopy, Polarization Mice, Inbred C57BL Disease Models, Animal Body Height Transcription, Genetic Seizures Bone Diseases, Developmental Chromosomes, Human, 6-12 and X Fetal Weight Protein Binding Mosaicism Heterozygote Detection Binding Sites Chromosomes, Human, Pair 15 Oculocerebrorenal Syndrome De Lange Syndrome Sequence Deletion Repressor Proteins Mutation, Missense

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