Short stature homeobox containing gene. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy38

Metacarpus Facial Bones Face Chromosomes, Human, X Arm Bones Bone and Bones X Chromosome Ring Chromosomes Chromosomes, Human, Pair 12 Chromosomes, Human, Y Chromosomes, Human, Pair 2 Y Chromosome Growth Plate Embryo, Nonmammalian Chromosomes, Human, Pair 15 Mesoderm Chromosomes, Human, 13-15 Head Spine Pituitary Gland Chromosomes, Human, Pair 4 Endoderm Extremities Meristem Ectoderm Chromosomes, Human, Pair 3 Prosencephalon Embryo, Mammalian Cells, Cultured Chick Embryo Eye Tibia Nervous System Skull Femur Chondrocytes Telencephalon Cell Line

Organisms4

Drosophila Chordata, Nonvertebrate Vertebrates Mice, Transgenic

Diseases73

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

Chemicals and Drugs44

Homeodomain Proteins Human Growth Hormone Growth Hormone Transcription Factors Insulin-Like Growth Factor I Otx Transcription Factors LIM-Homeodomain Proteins Receptors, Somatotropin MSX1 Transcription Factor Antennapedia Homeodomain Protein Goosecoid Protein Avian Proteins Codon, Nonsense Sodium Benzoate Oxymetholone Insulin-Like Growth Factor Binding Protein 3 Trans-Activators Protein Tyrosine Phosphatase, Non-Receptor Type 11 DNA Growth Hormone-Releasing Hormone Repressor Proteins Stanozolol Drosophila Proteins DNA Primers Cartilage Oligomeric Matrix Protein Matrilin Proteins DNA-Binding Proteins RNA, Messenger Pituitary Hormones Eye Proteins DNA, Complementary Nerve Tissue Proteins Hormones Somatomedins Zebrafish Proteins Genetic Markers Clonidine Plant Proteins Carrier Proteins Nuclear Proteins Proteins Extracellular Matrix Proteins Receptor, IGF Type 1 Recombinant Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment36

Body Height Age Determination by Skeleton Pedigree Growth Charts Karyotyping Chromosome Mapping Anthropometry In Situ Hybridization Facies DNA Mutational Analysis Bone Lengthening Osteogenesis, Distraction Body Weight Ilizarov Technique Hormone Replacement Therapy Reference Values External Fixators In Situ Hybridization, Fluorescence Sequence Analysis, DNA Cloning, Molecular Polymerase Chain Reaction Chromosome Banding Cohort Studies Retrospective Studies Sequence Alignment Blotting, Southern Body Mass Index Follow-Up Studies Birth Weight Cross-Sectional Studies Risk Factors Regression Analysis Amino Acid Substitution Prevalence Reverse Transcriptase Polymerase Chain Reaction Treatment Outcome

Psychiatry and Psychology7

Intellectual Disability Schizoid Personality Disorder Child Development Developmental Disabilities Adolescent Development Siblings Parents

Phenomena and Processes70

Genes, Homeobox Body Height Puberty Phenotype Gene Expression Regulation, Developmental Mutation Base Sequence Consanguinity Amino Acid Sequence Sex Chromosome Aberrations Genes, Recessive Bone Development Growth Chromosomes, Human, X Haploinsufficiency Homozygote Chromosome Deletion Mutation, Missense X Chromosome Heterozygote Mosaicism Ring Chromosomes Body Weight Genes, Dominant Chromosomes, Human, Pair 12 Exons Codon, Nonsense Gene Deletion Sequence Homology, Amino Acid Body Patterning Child Development Genetic Linkage Chromosomes, Human, Y Exome Chromosomes, Human, Pair 2 Y Chromosome Morphogenesis Point Mutation Cell Differentiation Adolescent Development Pregnancy Sequence Deletion Time Factors Chromosomes, Human, Pair 15 Gene Expression Genotype Chromosomes, Human, 13-15 Multigene Family Translocation, Genetic Promoter Regions, Genetic Chromosome Aberrations Chromosomes, Human, Pair 4 Gene Expression Regulation Body Mass Index Transcription, Genetic Trisomy Genetic Markers Polymorphism, Single Nucleotide Chromosomes, Human, Pair 3 Signal Transduction Frameshift Mutation Alleles Birth Weight Embryonic and Fetal Development Nutritional Status Phylogeny Microsatellite Repeats Amino Acid Substitution Genes, Insect Haploidy

Anthropology, Education, Sociology and Social Phenomena3

Siblings Parents Socioeconomic Factors

Information Science5

Molecular Sequence Data Base Sequence Amino Acid Sequence Phylogeny Prevalence

Named Groups5

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

Health Care15

Anthropometry Cohort Studies Family Health Retrospective Studies Age Factors Body Mass Index Follow-Up Studies Sex Factors Cross-Sectional Studies Risk Factors Nutritional Status Regression Analysis Prevalence Treatment Outcome Socioeconomic Factors

Geographicals1

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

Genes, Homeobox Growth Disorders Dwarfism Homeodomain Proteins Body Height Turner Syndrome Age Determination by Skeleton Osteochondrodysplasias Abnormalities, Multiple Dwarfism, Pituitary Noonan Syndrome Bone Diseases, Developmental Syndrome Human Growth Hormone Microcephaly Achondroplasia Puberty, Delayed Intellectual Disability Gonadal Dysgenesis, Mixed Growth Hormone Pedigree Hand Deformities, Congenital Puberty Metacarpus Transcription Factors Phenotype Hypertrichosis Molecular Sequence Data Gene Expression Regulation, Developmental Mutation Laron Syndrome Base Sequence Cephalopelvic Disproportion Facial Bones Consanguinity Growth Charts Puberty, Precocious Dysostoses Failure to Thrive Amino Acid Sequence Face Osteopoikilosis Sex Chromosome Aberrations Mental Retardation, X-Linked Genes, Recessive Cleidocranial Dysplasia Pelger-Huet Anomaly Craniofacial Abnormalities Karyotyping Lipoid Proteinosis of Urbach and Wiethe Insulin-Like Growth Factor I Chromosome Mapping Chromosome Disorders Anthropometry Infant, Newborn Limb Deformities, Congenital Bone Development Otx Transcription Factors Growth LIM-Homeodomain Proteins Pseudohypoparathyroidism In Situ Hybridization Chromosomes, Human, X Pigmentation Disorders Arm Bones Facies Brachydactyly DNA Mutational Analysis Optic Atrophy Haploinsufficiency Homozygote Bone and Bones Chromosome Deletion Hypopituitarism Schizoid Personality Disorder Mutation, Missense Bone Lengthening Musculoskeletal Abnormalities Osteogenesis, Distraction X Chromosome Receptors, Somatotropin Heterozygote Child Nutrition Disorders Foot Deformities, Congenital Mosaicism MSX1 Transcription Factor Endocrine System Diseases Ring Chromosomes Antennapedia Homeodomain Protein Goosecoid Protein Body Weight Genes, Dominant Chromosomes, Human, Pair 12 Avian Proteins Micrognathism Exons Ilizarov Technique Codon, Nonsense Chondrodysplasia Punctata Gene Deletion

No FAQ available that match "short stature homeobox containing gene"