The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray

Journal of the American Academy of Dermatology

Volumn 72, Issue 4, 2015, Pages 617-627

  Hand, Jennifer L ^a   Runke, Cassandra K ^a   Hodge, Jennelle C ^a,b  

^a MAYO CLINIC   (United States)

^b CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

chromosomal microarray; contiguous gene syndrome; eczema; Key words atopic dermatitis; steroid sulfatase deficiency; steroid sulfatase gene; X linked ichthyosis

Indexed keywords

STERYL SULFATASE;

ADOLESCENT; ADULT; ARTICLE; ATOPIC DERMATITIS; CHILD; CHROMOSOMAL MICROARRAY; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; DRY SKIN; ECZEMA; GENE DELETION; HUMAN; INFANT; MALE; MIDDLE AGED; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SYNDACTYLY; X LINKED ICHTHYOSIS; YOUNG ADULT; ABNORMALITIES, MULTIPLE; FEMALE; GENETIC SCREENING; GENETICS; ICHTHYOSIS, X-LINKED; INCIDENTAL FINDING; MICROARRAY ANALYSIS; PATHOLOGY; PHENOTYPE; PROCEDURES; SKIN; ULTRASTRUCTURE; X CHROMOSOME;

ABNORMALITIES, MULTIPLE; CHROMOSOMES, HUMAN, X; FEMALE; GENE DELETION; GENETIC TESTING; HUMANS; ICHTHYOSIS, X-LINKED; INCIDENTAL FINDINGS; MALE; MICROARRAY ANALYSIS; PHENOTYPE; SEQUENCE DELETION; SKIN; STERYL-SULFATASE;

EID: 84929514329     PISSN: 01909622     EISSN: 10976787     Source Type: Journal    
DOI: 10.1016/j.jaad.2014.12.020     Document Type: Article

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