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Volumn 126, Issue 12, 2006, Pages 2715-2717
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Generalized epidermolytic hyperkeratosis in two unrelated children from parents with localized linear form, and prenatal diagnosis [1]
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Author keywords
[No Author keywords available]
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Indexed keywords
DNA;
CASE REPORT;
CHILD PARENT RELATION;
CLINICAL FEATURE;
DIAGNOSTIC APPROACH ROUTE;
DISEASE PREDISPOSITION;
DNA DETERMINATION;
DNA EXTRACTION;
EPIDERMOLYTIC EPIDERMAL NAEVI;
GENE;
GENE MUTATION;
GENETIC SUSCEPTIBILITY;
HUMAN;
HYPERKERATOSIS;
KRT1 GENE;
KRT10 GENE;
LABORATORY TEST;
LETTER;
MUTATIONAL ANALYSIS;
NEVUS;
PRENATAL DIAGNOSIS;
PRIORITY JOURNAL;
ADULT;
DNA MUTATIONAL ANALYSIS;
FEMALE;
GLUTAMIC ACID;
HUMANS;
HYPERKERATOSIS, EPIDERMOLYTIC;
INFANT, NEWBORN;
ISOLEUCINE;
KERATIN-1;
KERATIN-10;
LYSINE;
MUTATION;
PHENYLALANINE;
PRENATAL DIAGNOSIS;
SKIN;
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EID: 33751073398
PISSN: 0022202X
EISSN: 15231747
Source Type: Journal
DOI: 10.1038/sj.jid.5700553 Document Type: Letter |
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Times cited : (29)
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References (7)
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