CHARGE: An association or a syndrome?

International Journal of Pediatric Otorhinolaryngology

Volumn 74, Issue 7, 2010, Pages 719-722

  Pampal, Arzu ^a  

^a UFUK UNIVERSITY   (Turkey)

Author keywords

CHARGE syndrome; CHD7 gene; Genetic basis

Indexed keywords

BINDING PROTEIN; CHROMODOMAIN HELICASE DNA BINDING PROTEIN 7; UNCLASSIFIED DRUG; CHD7 PROTEIN, HUMAN; DNA BINDING PROTEIN; HELICASE;

AUTOSOMAL DOMINANT INHERITANCE; CHD7 GENE; CHROMATIN ASSEMBLY AND DISASSEMBLY; CHROMOSOME 8Q; CLINICAL FEATURE; DISEASE ASSOCIATION; GENE; GENE EXPRESSION; GENE FUNCTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC COUNSELING; GROWTH REGULATION; HAPLOINSUFFICIENCY; HEREDITY; HETEROZYGOSITY; HUMAN; PATHOGENESIS; PHENOTYPE; POSTNATAL DEVELOPMENT; PRENATAL DEVELOPMENT; PRENATAL PERIOD; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN LOCALIZATION; REGULATORY MECHANISM; REVIEW; SYNDROME CHARGE; SYSTEMATIC REVIEW; FEMALE; GENETICS; HETEROZYGOTE; MUTATION; NOMENCLATURE; PHYSIOLOGY; PREGNANCY; PRENATAL DIAGNOSIS;

CHARGE SYNDROME; DNA HELICASES; DNA-BINDING PROTEINS; FEMALE; GENETIC COUNSELING; HETEROZYGOTE; HUMANS; MUTATION; PREGNANCY; PREIMPLANTATION DIAGNOSIS; PRENATAL DIAGNOSIS; TERMINOLOGY AS TOPIC;

EID: 79952018095     PISSN: 01655876     EISSN: 18728464     Source Type: Journal    
DOI: 10.1016/j.ijporl.2010.03.019     Document Type: Review

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