The genetics of hair shaft disorders

Journal of the American Academy of Dermatology

Volumn 59, Issue 1, 2008, Pages 1-22

  Cheng, Amy S ^a   Bayliss, Susan J ^b,c  

^a SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c ST LOUIS CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE;

ARGININOSUCCINIC ACID SYNTHETASE GENE; ARGININOSUCCINIC ACIDURIA; BJOERNSTAD SYNDROME; CARVAJAL SYNDROME; CHEMICAL ANALYSIS; CITRULLINEMIA; CONGENITAL HYPOTRICHOSIS; COSTELLO SYNDROME; CRANDALL SYNDROME; CURLY HAIR ANKYLOBLEPHARON AND NAIL DYSPLASIA SYNDROME; DIAGNOSTIC PROCEDURE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA REPAIR; ELECTRON MICROSCOPY; EXCISION REPAIR; GENE; GENETIC HETEROGENEITY; GENETICS; HAIR; HAIR DISEASE; HAIR FOLLICLE; HAIR GROWTH; HAIR ROOT; HAIR SHAFT DISORDER; HEARING LOSS; HEART RIGHT VENTRICLE DYSPLASIA; HHB1 GENE; HHB6 GENE; HISTOLOGY; HUMAN; LOOS ANAGEN SYNDROME; MENKES GENE; MENKES SYNDROME; MICROSCOPY; MOLECULAR BIOLOGY; MONILETHIX; NAXOS LIKE DISEASE; NETHERTON DISEASE; NOONAN SYNDROME; PHOTOSENSITIVITY; PRIORITY JOURNAL; REVIEW; RINGED HAIR; SKIN FRAGILITY; TRICHORRHEXIS; TRICHOTHIODYSTROPHY; UNCOMBABLE HAIR SYNDROME; WOLLY HAIR; XERODERMA PIGMENTOSUM COMPLEMENT B GENE; XERODERMA PIGMENTOSUM COMPLEMENT D GENE;

ADULT; CHILD; HAIR; HAIR DISEASES; HUMANS; INFANT; MENKES KINKY HAIR SYNDROME; MITOCHONDRIAL DISEASES; MUTATION; SYNDROME;

EID: 45149110868     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaad.2008.04.002     Document Type: Review

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