Types of dwarfism are skeletal dysplasias. Medical search. Frequent questions

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Anatomy9

Ribs Growth Plate Bone and Bones Cartilage Thorax Chondrocytes Femur Filamins Fetus

Organisms1

Mice, Mutant Strains

Diseases40

Dwarfism Bone Diseases, Developmental Osteochondrodysplasias Musculoskeletal Abnormalities Achondroplasia Thanatophoric Dysplasia Chondrodysplasia Punctata Short Rib-Polydactyly Syndrome Cleidocranial Dysplasia Exostoses, Multiple Hereditary Fibrous Dysplasia of Bone Abnormalities, Multiple Ectodermal Dysplasia Bronchopulmonary Dysplasia Osteogenesis Imperfecta Hajdu-Cheney Syndrome Fetal Diseases Limb Deformities, Congenital Syndrome Mucopolysaccharidosis IV Ellis-Van Creveld Syndrome Microcephaly Uterine Cervical Dysplasia Fibromuscular Dysplasia Craniosynostoses Growth Disorders Fibrous Dysplasia, Monostotic Fibrous Dysplasia, Polyostotic Hip Dysplasia, Canine Retinal Dysplasia Hip Dislocation, Congenital Micrognathism Barrett Esophagus Ectodermal Dysplasia 1, Anhidrotic Gigantism Arrhythmogenic Right Ventricular Dysplasia Malformations of Cortical Development Septo-Optic Dysplasia Osteopoikilosis Campomelic Dysplasia

Chemicals and Drugs18

Receptor, Fibroblast Growth Factor, Type 3 Matrilin Proteins Receptors, Fibroblast Growth Factor Cartilage Oligomeric Matrix Protein Natriuretic Peptide, C-Type Collagen Type XI Filamins Thyroid (USP)Growth Hormone TRPV Cation Channels Cyclic GMP-Dependent Protein Kinase Type II Brassinosteroids Steroids, Heterocyclic Extracellular Matrix Proteins Protein-Tyrosine Kinases Receptors, Somatotropin Cholestanols Gibberellins

Analytical, Diagnostic and Therapeutic Techniques and Equipment8

Ultrasonography, Prenatal Pedigree Prenatal Diagnosis Crown-Rump Length Biometry DNA Mutational Analysis Body Size Retrospective Studies

Phenomena and Processes14

Bone Development Mutation Genes, Recessive Consanguinity Phenotype Crown-Rump Length Mutation, Missense Pregnancy Gestational Age Heterozygote Base Sequence Exons Amino Acid Sequence Body Size

Disciplines and Occupations1

Genetic Counseling

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

Infant, Newborn

Health Care4

Crown-Rump Length Biometry Genetic Counseling Retrospective Studies

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Information Science Named Groups Health Care

Dwarfism Bone Diseases, Developmental Osteochondrodysplasias Musculoskeletal Abnormalities Achondroplasia Thanatophoric Dysplasia Chondrodysplasia Punctata Receptor, Fibroblast Growth Factor, Type 3 Ribs Short Rib-Polydactyly Syndrome Cleidocranial Dysplasia Exostoses, Multiple Hereditary Fibrous Dysplasia of Bone Growth Plate Abnormalities, Multiple Bone Development Ectodermal Dysplasia Bone and Bones Bronchopulmonary Dysplasia Osteogenesis Imperfecta Hajdu-Cheney Syndrome Fetal Diseases Limb Deformities, Congenital Mutation Syndrome Mucopolysaccharidosis IV Matrilin Proteins Cartilage Genes, Recessive Receptors, Fibroblast Growth Factor Consanguinity Thorax Ellis-Van Creveld Syndrome Cartilage Oligomeric Matrix Protein Chondrocytes Ultrasonography, Prenatal Phenotype Pedigree Prenatal Diagnosis Microcephaly Natriuretic Peptide, C-Type Uterine Cervical Dysplasia Collagen Type XI Crown-Rump Length Mutation, Missense Fibromuscular Dysplasia Femur Craniosynostoses Growth Disorders Fibrous Dysplasia, Monostotic Filamins Fibrous Dysplasia, Polyostotic Pregnancy Hip Dysplasia, Canine Infant, Newborn Gestational Age Biometry Retinal Dysplasia Hip Dislocation, Congenital Genetic Counseling Heterozygote Micrognathism Thyroid (USP)DNA Mutational Analysis Growth Hormone Barrett Esophagus Ectodermal Dysplasia 1, Anhidrotic Molecular Sequence Data TRPV Cation Channels Fetus Cyclic GMP-Dependent Protein Kinase Type II Gigantism Brassinosteroids Steroids, Heterocyclic Base Sequence Extracellular Matrix Proteins Arrhythmogenic Right Ventricular Dysplasia Malformations of Cortical Development Protein-Tyrosine Kinases Septo-Optic Dysplasia Exons Amino Acid Sequence Osteopoikilosis Receptors, Somatotropin Body Size Campomelic Dysplasia Cholestanols Retrospective Studies Gibberellins Mice, Mutant Strains

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