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BMC Medical Genetics, ISSN 1471-2350, 03/2018, Volume 19, Issue 1, pp. 41 - 41
Background: Ectodermal dysplasias (ED) are a group of diseases that affects the development or function of the teeth, hair, nails and exocrine and sebaceous... 
1q21.1 microdeletion syndrome | Bartsocas-Papas syndrome | CHUK | Cocoon syndrome | AEC | DEFECTS | RIPK4 | DISORDERS | GENETICS & HEREDITY | MALFORMATION | INTEGRATIVE GENOMICS VIEWER | COHORT | MUTATIONS | SPECTRUM | ASSOCIATION | Cleft Palate - diagnosis | Cleft Lip - diagnosis | Genetic Testing | Immunoglobulin G - blood | Humans | Eyelids - abnormalities | Child, Preschool | Male | Cleft Palate - genetics | Mutation, Missense | Genetic Variation | Microarray Analysis | Tumor Suppressor Proteins - genetics | Chromosomes, Human, Pair 1 - genetics | Immunologic Deficiency Syndromes - diagnosis | Abnormalities, Multiple - genetics | Chromosome Deletion | Megalencephaly - genetics | Amino Acid Sequence | Eye Abnormalities - diagnosis | Gene Frequency | Ectodermal Dysplasia - diagnosis | Protein-Serine-Threonine Kinases - genetics | Interferon Regulatory Factors - genetics | I-kappa B Kinase - genetics | Transcription Factors - genetics | Eye Abnormalities - genetics | Cleft Lip - genetics | Phenotype | Pedigree | Immunologic Deficiency Syndromes - genetics | Heterozygote | Ectodermal Dysplasia - genetics | Genetic disorders | Genetic variation | Immunological deficiency syndromes | Genetic aspects | Research | Ectodermal dysplasia | Infection | Dysplasia | DNA microarrays | Immunodeficiency | Development and progression | Skin | Health aspects | Index Medicus | Bartsocas–Papas syndrome
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