Association of microcephaly and café-au-lait spots in a patient with ring chromosome 12 syndrome

Clinical Dysmorphology

Volumn 14, Issue 3, 2005, Pages 141-143

  Zen, P R G ^a   Pinto, L L C ^a   Graziadio, C ^a   Pereira, V B ^a   Paskulin, Giorgio Adriano ^a  

^a UNIVERSIDADE FEDERAL DE CIÊNCIAS DA SAÚDE DE PORTO ALEGRE   (Brazil)

Author keywords

Cafe au lait spots; Microcephaly; Ring chromosome 12

Indexed keywords

ARTICLE; BLOOD; CAFE AU LAIT SPOT; CASE REPORT; CHROMOSOME 12; CHROMOSOME ANALYSIS; CLINICAL FEATURE; CLINODACTYLY; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; FACE MALFORMATION; FINGER MALFORMATION; HIGH ARCHED PALATE; HUMAN; HUMAN CELL; MALE; MICROCEPHALY; NOSE MALFORMATION; PALPEBRAL FISSURE ANOMALY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; RING CHROMOSOME; RING CHROMOSOME 12 SYNDROME; SCHOOL CHILD;

ABNORMALITIES, MULTIPLE; CAFE-AU-LAIT SPOTS; CHILD; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 12; DEVELOPMENTAL DISABILITIES; EAR; FINGERS; HUMANS; KARYOTYPING; MALE; MICROCEPHALY; RING CHROMOSOMES; SYNDROME;

EID: 21244478985     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200507000-00007     Document Type: Article

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