Severe phenotype with growth retardation. Medical search. Frequent questions

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Anatomy28

Ring Chromosomes Placenta Fibroblasts Cells, Cultured Growth Plate Brain Cell Line Fetus Arm Bones Embryo, Mammalian Umbilical Arteries X Chromosome Muscle, Skeletal Bone and Bones Liver Face Chromosomes, Human, X Chromosomes, Human, Pair 15 Skull Head Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 4 Chondrocytes Chromosomes, Human, Pair 7 Fetal Blood Neurons Trophoblasts Kidney

Organisms10

Mice, Knockout Mice, Transgenic Mice, Inbred C57BL Zebrafish Animals, Newborn Mice, Mutant Strains Arabidopsis Rats, Wistar Rats, Sprague-Dawley Plants, Genetically Modified

Diseases76

Fetal Growth Retardation Growth Disorders Intellectual Disability Abnormalities, Multiple Syndrome Mental Retardation, X-Linked Corneal Dystrophy, Juvenile Epithelial of Meesmann Ring Chromosomes Microcephaly Facies Muscular Dystrophies Fetal Death Disease Models, Animal Dwarfism Fetal Weight Birth Weight Fragile X Syndrome Peroxisomal Disorders Abnormalities, Drug-Induced Body Weight Pregnancy Complications Failure to Thrive Chromosome Disorders Chromosome Deletion Nutrition Disorders Fetal Diseases Psychomotor Disorders Trisomy Embryo Loss Chromosome Aberrations Genetic Predisposition to Disease Craniofacial Abnormalities Blepharophimosis Obstetric Labor, Premature Oligohydramnios Skin Abnormalities Congenital Abnormalities Bone Diseases, Developmental Placental Insufficiency Fetal Hypoxia Prenatal Exposure Delayed Effects Rubinstein-Taybi Syndrome De Lange Syndrome Puberty, Delayed Pre-Eclampsia Hand Deformities, Congenital Sex Chromosome Aberrations Fetal Resorption Foot Deformities, Congenital Nijmegen Breakage Syndrome Osteochondrodysplasias Weight Gain Carbohydrate Metabolism, Inborn Errors Uniparental Disomy Placenta Diseases Abortion, Threatened Noma Gingival Hyperplasia Micrognathism Fetal Alcohol Spectrum Disorders Ichthyosis Pregnancy Complications, Cardiovascular Deficiency Diseases Translocation, Genetic Protein-Energy Malnutrition Pregnancy in Diabetics Heart Defects, Congenital Turner Syndrome Ataxia Child Nutrition Disorders Barth Syndrome Malnutrition Muscle Hypotonia Glycogen Storage Disease Type I Electric Injuries Cleft Palate

Chemicals and Drugs29

Fragile X Mental Retardation Protein Codon, Nonsense RNA, Messenger Transcription Factors DNA-Binding Proteins Nuclear Proteins DNA Primers Dystrophin Homeodomain Proteins Carrier Proteins Membrane Proteins Proteins Zebrafish Proteins Eye Proteins DNA Teratogens Growth Hormone Insulin-Like Growth Factor I Nerve Tissue Proteins Zinc Repressor Proteins Arabidopsis Proteins Human Growth Hormone Cell Cycle Proteins Glucocorticoids DNA Helicases RNA-Binding Proteins Insulin Placental Hormones

Analytical, Diagnostic and Therapeutic Techniques and Equipment46

Pedigree Physiognomy DNA Mutational Analysis Facies Disease Models, Animal Chromosome Mapping Polymerase Chain Reaction Fetal Weight Birth Weight Genetic Complementation Test Body Height Sequence Analysis, DNA Body Weight Genetic Testing In Situ Hybridization Gene Targeting Cordocentesis Pregnancy Outcome Karyotyping Age Determination by Skeleton Organ Size Prenatal Diagnosis Crosses, Genetic In Situ Hybridization, Fluorescence Amino Acid Substitution Reverse Transcriptase Polymerase Chain Reaction Severity of Illness Index Anthropometry Ultrasonography, Prenatal Chromosome Banding Immunohistochemistry Blotting, Western Cloning, Molecular Models, Genetic Ultrasonography Crown-Rump Length Cephalometry Gene Expression Profiling Mutagenesis, Insertional Transfection Ultrasonography, Doppler, Pulsed Models, Biological Sequence Alignment Oligonucleotide Array Sequence Analysis Diet, Protein-Restricted Gene Knockout Techniques

Psychiatry and Psychology6

Intellectual Disability Developmental Disabilities Psychomotor Disorders Child Development Fathers Food Deprivation

Phenomena and Processes82

Phenotype Mutation Pregnancy Homozygote Genotype Heterozygote Ring Chromosomes Base Sequence Exons Mutation, Missense Growth Alleles Mosaicism Gene Deletion Genes, Recessive Frameshift Mutation Amino Acid Sequence Point Mutation Codon, Nonsense Gene Expression Regulation, Developmental Gestational Age Fetal Weight Birth Weight Sequence Deletion Embryonic and Fetal Development Body Height Genes, Dominant Gene Expression Body Weight Signal Transduction Fetal Development Consanguinity Pregnancy Outcome Polymorphism, Single-Stranded Conformational Introns Genomic Imprinting Chromosome Deletion Haplotypes Organ Size Trisomy Placental Circulation Maternal-Fetal Exchange Chromosome Aberrations Bone Development Genetic Predisposition to Disease X Chromosome Amino Acid Substitution Genes, Lethal Cell Differentiation Time Factors Gene Expression Regulation Protein Structure, Tertiary Cell Division Promoter Regions, Genetic Sex Chromosome Aberrations Litter Size Cell Proliferation Chromosomes, Human, X Genetic Linkage Weight Gain Uniparental Disomy Embryonic Development Transcription, Genetic Chromosomes, Human, Pair 15 Pregnancy Trimester, Third Child Development Apoptosis Birefringence Crown-Rump Length Gene Expression Regulation, Plant Translocation, Genetic Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 7 Mutagenesis, Insertional Protein Binding Transfection Growth and Development Pregnancy Trimester, Second DNA Methylation Diet, Protein-Restricted Fertility

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena2

Ethnology Fathers

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups6

Infant, Newborn Infant, Small for Gestational Age Infant, Low Birth Weight Infant, Postmature Infant, Premature Fathers

Health Care8

Age of Onset Genetic Testing Family Health Severity of Illness Index Anthropometry Crown-Rump Length Cephalometry Maternal Exposure

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

Fetal Growth Retardation Phenotype Growth Disorders Intellectual Disability Mutation Pedigree Abnormalities, Multiple Syndrome Mental Retardation, X-Linked Pregnancy Physiognomy Molecular Sequence Data Homozygote Genotype Heterozygote Corneal Dystrophy, Juvenile Epithelial of Meesmann Fragile X Mental Retardation Protein DNA Mutational Analysis Infant, Newborn Ring Chromosomes Base Sequence Exons Mutation, Missense Mice, Knockout Microcephaly Growth Alleles Mosaicism Gene Deletion Genes, Recessive Facies Frameshift Mutation Amino Acid Sequence Mice, Transgenic Muscular Dystrophies Point Mutation Fetal Death Codon, Nonsense Mice, Inbred C57BL Gene Expression Regulation, Developmental Disease Models, Animal Chromosome Mapping RNA, Messenger Gestational Age Placenta Dwarfism Transcription Factors Polymerase Chain Reaction Fetal Weight Birth Weight Fragile X Syndrome DNA-Binding Proteins Genetic Complementation Test Sequence Deletion Peroxisomal Disorders Embryonic and Fetal Development Abnormalities, Drug-Induced Age of Onset Body Height Genes, Dominant Fibroblasts Gene Expression Infant, Small for Gestational Age Nuclear Proteins DNA Primers Dystrophin Cells, Cultured Sequence Analysis, DNA Body Weight Homeodomain Proteins Pregnancy Complications Genetic Testing Zebrafish In Situ Hybridization Failure to Thrive Growth Plate Signal Transduction Gene Targeting Brain Cell Line Cordocentesis Carrier Proteins Membrane Proteins Fetal Development Developmental Disabilities Proteins Family Health Zebrafish Proteins Eye Proteins Infant, Low Birth Weight Consanguinity DNA Fetus Pregnancy Outcome Animals, Newborn Mice, Mutant Strains Arm Bones Polymorphism, Single-Stranded Conformational Teratogens Karyotyping

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