An unusual human mosaic for skin pigmentation

Genetic Counseling

Volumn 13, Issue 3, 2002, Pages 281-287

  Stoll, Claude ^a   Alembik, Y ^a   Grosshans, E ^a   De Saint Martin, A ^a  

^a HÔPITAL DE HAUTEPIERRE   (France)

Author keywords

Congenital anomalies; Hyperpigmentation; Hypopigmentation; Mosaicism; Pigmentary Disorder; Translocation

Indexed keywords

ARTICLE; CASE REPORT; CHILD DEVELOPMENT; CHROMOSOME 12Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME MOSAICISM; CHROMOSOME TRANSLOCATION; CLINICAL EXAMINATION; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; FACE DYSMORPHIA; FACIES; FIBROBLAST; HIRSUTISM; HUMAN; HYPERPIGMENTATION; KARYOTYPING; MALE; PHILTRUM; PREGNANCY; PRESCHOOL CHILD; SKIN DEFECT; SKIN PIGMENTATION;

CHILD, PRESCHOOL; HUMANS; INFANT, NEWBORN; KARYOTYPING; MALE; MOSAICISM; PIGMENTATION DISORDERS; TRANSLOCATION, GENETIC;

EID: 0036387945     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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