Follow-up of adult males with chromosome 18p deletion

European Journal of Medical Genetics

Volumn 48, Issue 2, 2005, Pages 189-193

  De Ravel, Thomy J L ^a   Thiry, Paul ^b   Fryns, Jean Pierre ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b Sint Oda Dienstencentrum ^*  (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANAMNESIS; ARTICLE; CASE REPORT; CHROMOSOME 18P; CHROMOSOME DELETION; CHROMOSOME DELETION 18P; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GENETIC DISORDER; HUMAN; INTELLIGENCE QUOTIENT; KARYOTYPE; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; PSYCHOMOTOR RETARDATION;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; FOLLOW-UP STUDIES; HUMANS; MALE; MENTAL RETARDATION; MIDDLE AGED; PHENOTYPE; SYNDROME;

GENETTA;

EID: 18844416870     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2005.01.024     Document Type: Article

References (13)

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