Syndromic and nonsyndromic patients with craniosynostosis. Medical search. Frequent questions

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Anatomy18

Cranial Sutures Skull Frontal Bone Parietal Bone Vestibular Aqueduct Osteoblasts Zygoma Dura Mater Facial Bones Cochlea Chromosomes, Human, X Orbit Chromosomes, Human, Pair 7 Sphenoid Bone Cranial Sinuses Cochlear Duct Neural Crest Ear, Inner

Diseases29

Craniosynostoses Acrocephalosyndactylia Craniofacial Dysostosis Cleft Lip Cleft Palate Hearing Loss Deafness Syndrome Hearing Loss, Sensorineural Mental Retardation, X-Linked Foot Deformities, Congenital Craniofacial Abnormalities Bone Diseases, Developmental Abnormalities, Multiple Syndactyly Synostosis Hypertelorism Hearing Loss, Bilateral Maxillofacial Abnormalities Holoprosencephaly Intellectual Disability Usher Syndromes Hand Deformities, Congenital Micrognathism Velopharyngeal Insufficiency Pierre Robin Syndrome Microphthalmos Articulation Disorders Chromosome Duplication

Chemicals and Drugs16

Receptor, Fibroblast Growth Factor, Type 2 Receptor, Fibroblast Growth Factor, Type 3 Twist Transcription Factor Receptors, Fibroblast Growth Factor Connexins Receptor, Fibroblast Growth Factor, Type 1 MARVEL Domain Containing 2 Protein SOXD Transcription Factors Receptor Protein-Tyrosine Kinases Axin Protein Transforming Growth Factor beta3 Core Binding Factor Alpha 1 Subunit Codon, Nonsense Genetic Markers Fibroblast Growth Factors Transcription Factor Brn-3C

Analytical, Diagnostic and Therapeutic Techniques and Equipment10

Pedigree DNA Mutational Analysis Audiometry Chromosome Mapping Reconstructive Surgical Procedures Case-Control Studies Sequence Analysis, DNA Craniotomy Neurosurgical Procedures Genetic Testing

Psychiatry and Psychology2

Intellectual Disability Fathers

Phenomena and Processes27

Genes, Recessive Mutation Consanguinity Cystine Knot Motifs Genetic Linkage Mutation, Missense Genes, Dominant Lod Score Phenotype Heterozygote Osteogenesis Exome Chromosomes, Human, X Point Mutation Homozygote Chromosomes, Human, Pair 7 Base Sequence Frameshift Mutation Intracranial Pressure Codon, Nonsense Amino Acid Sequence Gene Expression Regulation, Developmental Haplotypes Genetic Markers Genetic Heterogeneity Polymorphism, Single Nucleotide Chromosome Duplication

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups2

Infant, Newborn Fathers

Health Care3

Case-Control Studies Checklist Genetic Testing

Geographicals1

Anatomy 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

Craniosynostoses Cranial Sutures Acrocephalosyndactylia Craniofacial Dysostosis Skull Receptor, Fibroblast Growth Factor, Type 2 Cleft Lip Cleft Palate Hearing Loss Frontal Bone Parietal Bone Deafness Pedigree Receptor, Fibroblast Growth Factor, Type 3 Syndrome Twist Transcription Factor Hearing Loss, Sensorineural Genes, Recessive Receptors, Fibroblast Growth Factor Mutation Vestibular Aqueduct Mental Retardation, X-Linked Consanguinity Foot Deformities, Congenital DNA Mutational Analysis Cystine Knot Motifs Craniofacial Abnormalities Genetic Linkage Mutation, Missense Genes, Dominant Connexins Bone Diseases, Developmental Lod Score Abnormalities, Multiple Syndactyly Phenotype Audiometry Osteoblasts Zygoma Heterozygote Synostosis Dura Mater Chromosome Mapping Hypertelorism Osteogenesis Facial Bones Exome Hearing Loss, Bilateral Reconstructive Surgical Procedures Maxillofacial Abnormalities Holoprosencephaly Intellectual Disability Cochlea Usher Syndromes Hand Deformities, Congenital Receptor, Fibroblast Growth Factor, Type 1 Infant, Newborn Chromosomes, Human, X Point Mutation Orbit Molecular Sequence Data Micrognathism Velopharyngeal Insufficiency Homozygote Chromosomes, Human, Pair 7 MARVEL Domain Containing 2 Protein SOXD Transcription Factors Case-Control Studies Base Sequence Pakistan Receptor Protein-Tyrosine Kinases Axin Protein Sphenoid Bone Fathers Cranial Sinuses Transforming Growth Factor beta3 Pierre Robin Syndrome Sequence Analysis, DNA Frameshift Mutation Core Binding Factor Alpha 1 Subunit Intracranial Pressure Codon, Nonsense Amino Acid Sequence Cochlear Duct Neural Crest Microphthalmos Checklist Articulation Disorders Ear, Inner Craniotomy Gene Expression Regulation, Developmental Haplotypes Genetic Markers Neurosurgical Procedures Genetic Heterogeneity Fibroblast Growth Factors Polymorphism, Single Nucleotide Genetic Testing Chromosome Duplication Transcription Factor Brn-3C

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