SCOPUS 정보 검색 플랫폼

Volumn 51, Issue 9, 2000, Pages 688-692

Hypomelanosis of Ito in a case of trisomy 9 mosaicism (46,XX/46,XX,t(9;9) (p24;p24)): Spontaneous resolution of skin lesions during childhood;Hypomelanosis Ito bei translokationstrisomie 9/mosaik (46,XX/46,XX, t(9;9)(p24;p24)): Spontane ruckbildung im kindesalter

(3) Dereser Dennl, M a Brude, E a Konig R a

a UNIVERSITY HOSPITAL FRANKFURT (Germany)

Author keywords

Genetic mosaicism; Hypomelanosis Ito

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME MOSAICISM; CLINICAL FEATURE; DISEASE ASSOCIATION; ELECTROENCEPHALOGRAM; FEMALE; HUMAN; INCONTINENTIA PIGMENTI; KARYOTYPING; NUCLEAR MAGNETIC RESONANCE IMAGING; PARTIAL TRISOMY 9; SKIN MANIFESTATION;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 9; DIAGNOSIS, DIFFERENTIAL; FEMALE; FOLLOW-UP STUDIES; HUMANS; MENTAL RETARDATION; PIGMENTATION DISORDERS; REMISSION, SPONTANEOUS; TRANSLOCATION, GENETIC; TRISOMY;

EID: 0033824671 PISSN: 00178470 EISSN: None Source Type: Journal
DOI: 10.1007/s001050051197 Document Type: Article

Times cited : (12)

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