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Anatomy40

Metacarpus Facial Bones Face Chromosomes, Human, X Bone and Bones Arm Bones Skeleton Chromosomes, Human, Pair 12 Diastema Ring Chromosomes Spine X Chromosome Eyebrows Y Chromosome Chromosomes, Human, Y Growth Plate Leg Pelvis Chromosomes, Human, Pair 15 Wrist Toes Chromosomes, Human, Pair 2 Chromosomes, Human, 1-3 Femur Head Filamins Skull Chromosomes, Human, 13-15 Chromosomes, Human, Pair 7 Ribs Fingers Chromosomes, Human, Pair 3 Pituitary Gland Arm Chromosomes, Human, Pair 4 Tibia Chromosomes, Human, Pair 18 Head Femur Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 1

Organisms1

Diseases89

Growth Disorders Dwarfism Turner Syndrome Osteochondrodysplasias Dwarfism, Pituitary Noonan Syndrome Bone Diseases, Developmental Abnormalities, Multiple Syndrome Puberty, Delayed Microcephaly Achondroplasia Gonadal Dysgenesis, Mixed Intellectual Disability Hypertrichosis Hand Deformities, Congenital Puberty, Precocious Sex Chromosome Aberrations Body Weight Laron Syndrome Cephalopelvic Disproportion Mental Retardation, X-Linked Dysostoses Failure to Thrive Osteopoikilosis Sex Chromosome Disorders Cleidocranial Dysplasia Pelger-Huet Anomaly Eunuchism Limb Deformities, Congenital Lipoid Proteinosis of Urbach and Wiethe Chromosome Disorders Weill-Marchesani Syndrome Hypopituitarism Child Nutrition Disorders Gonadal Dysgenesis Pseudohypoparathyroidism Craniofacial Abnormalities Pigmentation Disorders Rothmund-Thomson Syndrome Gonadal Dysgenesis, 46,XY Hypogonadism Chromosome Deletion Brachydactyly Optic Atrophy Diastema Chondrodysplasia Punctata Ellis-Van Creveld Syndrome Musculoskeletal Abnormalities Klinefelter Syndrome Thinness Ring Chromosomes Micrognathism Myokymia Endocrine System Diseases Leg Length Inequality Genu Valgum Scoliosis Acidosis, Renal Tubular Birth Weight Skin Abnormalities Nephrocalcinosis Prader-Willi Syndrome Mouth Abnormalities Muscle Hypotonia Rubinstein-Taybi Syndrome Foot Deformities, Congenital Livedo Reticularis Exocrine Pancreatic Insufficiency Nutrition Disorders Fetal Growth Retardation Malnutrition Fibrous Dysplasia, Polyostotic Marfan Syndrome Chromosome Aberrations Adrenal Hyperplasia, Congenital Progeria Neurofibromatosis 1 Obesity Rare Diseases Celiac Disease Learning Disorders Heart Defects, Congenital Trisomy Translocation, Genetic Genetic Diseases, X-Linked Osteogenesis Imperfecta Hypothyroidism Overweight

Chemicals and Drugs26

Growth Hormone Insulin-Like Growth Factor I Homeodomain Proteins Receptors, Somatotropin Insulin-Like Growth Factor Binding Protein 3 Codon, Nonsense Sodium Benzoate HMGA2 Protein Oxymetholone Growth Hormone-Releasing Hormone Protein Tyrosine Phosphatase, Non-Receptor Type 11 Gibberellins Cartilage Oligomeric Matrix Protein Stanozolol Matrilin Proteins Pituitary Hormones Filamins Hormones Somatomedins Ethinyl Estradiol Protein Tyrosine Phosphatases, Non-Receptor Clonidine Receptor, IGF Type 1 Aromatase Inhibitors Extracellular Matrix Proteins Contractile Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment37

Age Determination by Skeleton Anthropometry Pedigree Growth Charts Body Weight Karyotyping Reference Values Obstetric Surgical Procedures Body Size Bone Lengthening Body Mass Index Chromosome Mapping DNA Mutational Analysis Skinfold Thickness Osteogenesis, Distraction Thinness Hormone Replacement Therapy Cohort Studies Cephalometry Body Constitution Ilizarov Technique Birth Weight Cross-Sectional Studies Regression Analysis External Fixators Risk Factors Follow-Up Studies Biometry In Situ Hybridization, Fluorescence Chromosome Banding Retrospective Studies Genome-Wide Association Study Prevalence Obesity Genetic Association Studies Overweight Amino Acid Substitution

Psychiatry and Psychology11

Intellectual Disability Child Development Adolescent Development Schizoid Personality Disorder Developmental Disabilities Siblings Human Development Parents Learning Disorders Mothers Family

Phenomena and Processes72

Puberty Sex Chromosome Aberrations Phenotype Body Weight Consanguinity Bone Development Genes, Recessive Mutation Chromosomes, Human, X Child Development Body Size Body Mass Index Haploinsufficiency Chromosome Deletion Chromosomes, Human, Pair 12 Adolescent Development Mosaicism Mutation, Missense Skinfold Thickness Thinness Ring Chromosomes X Chromosome Homozygote Genetic Linkage Genes, Dominant Heterozygote Y Chromosome Body Constitution Chromosomes, Human, Y Codon, Nonsense Birth Weight Body Composition Multifactorial Inheritance Nutritional Status Exome Sex Characteristics Chromosomes, Human, Pair 15 Exons Human Development Pregnancy Gene Deletion Genotype Lod Score Chromosomes, Human, Pair 2 Polymorphism, Single Nucleotide Chromosomes, Human, 1-3 Chromosome Aberrations Chromosomes, Human, 13-15 Point Mutation Chromosomes, Human, Pair 7 Obesity Trisomy Chromosomes, Human, Pair 3 Sequence Deletion Bone Density Translocation, Genetic Base Sequence Aging Child Nutritional Physiological Phenomena Time Factors Parity Chromosomes, Human, Pair 4 Frameshift Mutation Chromosomes, Human, Pair 18 Microsatellite Repeats Maternal Age Overweight Chromosomes, Human, Pair 9 Genetic Variation Chromosomes, Human, Pair 1 Amino Acid Substitution Gene Expression Regulation, Plant

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena8

Anthropology, Physical Forensic Anthropology Siblings Parents Socioeconomic Factors Mothers Social Class Family

Information Science3

Prevalence Molecular Sequence Data Base Sequence

Named Groups9

Infant, Newborn Infant, Small for Gestational Age Siblings Parents Mothers European Continental Ancestry Group Infant, Low Birth Weight Asian Continental Ancestry Group Twins, Dizygotic

Health Care22

Anthropometry Body Mass Index Sex Factors Age Factors Cohort Studies Cephalometry Cross-Sectional Studies Regression Analysis Nutritional Status Risk Factors Follow-Up Studies Biometry Family Health Retrospective Studies Socioeconomic Factors Genome-Wide Association Study Prevalence Social Class Parity Genetic Counseling Educational Status Maternal Age

Geographicals4

Saudi Arabia Guatemala Peru Brazil

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 Geographicals

Growth Disorders Dwarfism Turner Syndrome Age Determination by Skeleton Osteochondrodysplasias Dwarfism, Pituitary Noonan Syndrome Bone Diseases, Developmental Abnormalities, Multiple Syndrome Puberty, Delayed Microcephaly Achondroplasia Gonadal Dysgenesis, Mixed Puberty Growth Hormone Intellectual Disability Metacarpus Anthropometry Hypertrichosis Pedigree Hand Deformities, Congenital Puberty, Precocious Sex Chromosome Aberrations Phenotype Growth Charts Body Weight Laron Syndrome Consanguinity Cephalopelvic Disproportion Mental Retardation, X-Linked Dysostoses Infant, Newborn Bone Development Facial Bones Failure to Thrive Face Genes, Recessive Osteopoikilosis Mutation Insulin-Like Growth Factor I Karyotyping Sex Chromosome Disorders Chromosomes, Human, X Cleidocranial Dysplasia Pelger-Huet Anomaly Reference Values Child Development Obstetric Surgical Procedures Eunuchism Limb Deformities, Congenital Body Size Anthropology, Physical Lipoid Proteinosis of Urbach and Wiethe Chromosome Disorders Weill-Marchesani Syndrome Hypopituitarism Child Nutrition Disorders Bone and Bones Gonadal Dysgenesis Pseudohypoparathyroidism Bone Lengthening Craniofacial Abnormalities Pigmentation Disorders Rothmund-Thomson Syndrome Gonadal Dysgenesis, 46,XY Homeodomain Proteins Arm Bones Body Mass Index Hypogonadism Haploinsufficiency Skeleton Chromosome Deletion Chromosomes, Human, Pair 12 Sex Factors Brachydactyly Optic Atrophy Adolescent Development Mosaicism Mutation, Missense Diastema Chromosome Mapping Chondrodysplasia Punctata DNA Mutational Analysis Schizoid Personality Disorder Ellis-Van Creveld Syndrome Receptors, Somatotropin Musculoskeletal Abnormalities Skinfold Thickness Osteogenesis, Distraction Klinefelter Syndrome Thinness Ring Chromosomes Age Factors Micrognathism Spine Insulin-Like Growth Factor Binding Protein 3 X Chromosome Myokymia Homozygote

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