Ring chromosome 17: Phenotype variation by deletion size

Clinical Genetics

Volumn 64, Issue 4, 2003, Pages 361-365

  Shashi, Vandana ^a   White, J R ^b   Pettenati, M J ^a   Root, S K ^c   Bell, W L ^a  

^a WAKE FOREST SCHOOL OF MEDICINE   (United States)

^b MINCEP Epilepsy Care   (United States)

^c UNIVERSITY OF NEW MEXICO SCHOOL OF MEDICINE   (United States)

Author keywords

Caf au lait spots; Chromosome 17; Mental retardation; Ring chromosome 17

Indexed keywords

ADOLESCENT; ADULT; AGYRIA; ARTICLE; CAFE AU LAIT SPOT; CASE REPORT; CHROMOSOME 17; CHROMOSOME ABERRATION; CYTOGENETICS; FEMALE; GENE DELETION; GROWTH RETARDATION; HUMAN; LIFE EXPECTANCY; MALE; MEDICAL LITERATURE; MENTAL DEFICIENCY; MILLER DIEKER SYNDROME; PHENOTYPIC VARIATION; PRIORITY JOURNAL; RETROSPECTIVE STUDY; RING CHROMOSOME; SEIZURE; SHORT STATURE; SKIN MANIFESTATION;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; ELECTROENCEPHALOGRAPHY; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MAGNETIC RESONANCE IMAGING; MALE; MENTAL RETARDATION; PHENOTYPE; RING CHROMOSOMES; SYNDROME;

ACRONICTA LEPORINA;

EID: 0141886851     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2003.00146.x     Document Type: Article

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