Skin pigmentary anomalies in a mosaic form of partial tetrasomy 3q [11]

Journal of Medical Genetics

Volumn 37, Issue 9, 2000, Pages 723-725

  Kroisel, P M ^a   Petek, E ^a   Wagner, K ^a  

^a UNIVERSITY OF GRAZ   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; CASE REPORT; CHILD; CHROMOSOME 3Q; CHROMOSOME DUPLICATION; CHROMOSOME MAP; CLINICAL FEATURE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DOSAGE; HUMAN; HYPERPIGMENTATION; INTRAUTERINE GROWTH RETARDATION; KARYOTYPE; LETTER; LYMPHOCYTE; MALE; MOLECULAR CLONING; MOSAICISM; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PIGMENT DISORDER; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT; SKIN PIGMENTATION; TETRASOMY;

CASE REPORT; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 3; HUMAN; HYPERPIGMENTATION; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MOSAICISM;

EID: 0033832875     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (4)

1. Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q
2. Lyonization and the lines of Blaschko
3. Linear and whorled hypermelanosis
4. Assignment of the gene for human melanoma-associated antigen p97 to chromosome 3