Clinical and Pathologic Correlations in Genetically Distinct Forms of Atrichia

Archives of Dermatology

Volumn 139, Issue 12, 2003, Pages 1591-1596

  Zlotogorski, Abraham ^a   Hochberg, Ze'Ev ^e   Mirmirani, Paradi ^d   Metzker, Arye ^b   Ben Amitai, Dan ^c   Martinez Mir, Amalia ^f   Panteleyev, Andrey A ^f   Christiano, Angela M ^f  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^b TEL AVIV SOURASKY MEDICAL CENTER   (Israel)

^c RABIN MEDICAL CENTER   (Israel)

^d UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^e MEYER CHILDREN S HOSPITAL   (Israel)

^f Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADOLESCENT; ADULT; ARTICLE; ATRICHIA; ATRICHIA WITH PAPULAR LESION; CHILD; CHROMOSOME 12Q; CHROMOSOME 8P; CLINICAL ARTICLE; CLINICAL FEATURE; FAMILY STUDY; FEMALE; GENE; GENE FUNCTION; GENE MUTATION; GENETIC DISORDER; GENETIC VARIABILITY; HAIR DISEASE; HAIRLESS GENE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; MALE; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; VITAMIN D RECEPTOR GENE; VITAMIN D RESISTANT RICKETS; VITAMIN D RESISTANT RICKETS TYPE IIA;

ADOLESCENT; ADULT; ALOPECIA; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 8; CONSANGUINITY; FEMALE; HETEROZYGOTE DETECTION; HUMANS; MALE; MIDDLE AGED; MUTATION; PHENOTYPE; RECEPTORS, CALCITRIOL; RICKETS; SKIN DISEASES, PAPULOSQUAMOUS; TWINS, DIZYGOTIC;

EID: 0346125403     PISSN: 0003987X     EISSN: None     Source Type: Journal    
DOI: 10.1001/archderm.139.12.1591     Document Type: Article

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