Phylloid hypomelanosis and mosaic partial trisomy 13: Two cases that provide further evidence of a distinct clinicogenetic entity

Archives of Dermatology

Volumn 145, Issue 5, 2009, Pages 576-578

  González Enseñat, M Antonia ^a   Vicente, Asunción ^a   Poo, Pilar ^a   Catalá, Vicenç ^c   Pérez Iribarne, M Mar ^a   Fuster, Carme ^b   Geán, Esther ^a   Happle, Rudolf ^d  

^a UNIVERSITY OF BARCELONA   (Spain)

^b UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^c Prenatal Genetics   (Spain)

^d PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 13Q; CLINICAL FEATURE; CLINODACTYLY; CYTOGENETICS; FEMALE; FISTULA; HUMAN; HYPOMELANOSIS; KARYOTYPE 46,XX; MENTAL DEFICIENCY; MOSAICISM; OLIGODONTIA; PARTIAL TRISOMY 13; PHENOTYPE; PHYLLOID HYPOMELANOSIS; PRIORITY JOURNAL; SCHOOL CHILD; SCOLIOSIS; SEIZURE; SKIN FIBROBLAST; SYNDACTYLY; SYRINGOMYELIA; TELANGIECTASIA; TETHERED CORD SYNDROME; TETRASOMY; TOOTH MALFORMATION;

ADOLESCENT; CHILD; CHROMOSOMES, HUMAN, PAIR 13; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; HYPOPIGMENTATION; IN SITU HYBRIDIZATION, FLUORESCENCE; MOSAICISM; PHENOTYPE; SKIN PIGMENTATION; TRISOMY;

EID: 66149086851     PISSN: 0003987X     EISSN: 15383652     Source Type: Journal    
DOI: 10.1001/archdermatol.2009.37     Document Type: Article

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