Familial deletion of chromosome 18 (p11.2)

Annales de Genetique

Volumn 39, Issue 4, 1996, Pages 201-204

  Velagaleti, G V N ^a   Harris, S ^a   Carpenter, N J ^a   Coldwell, J ^a   Say, B ^a  

^a UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

Author keywords

Chromosome 18; Deletion; Recurrence risk

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 18P; CHROMOSOME DELETION; CLINICAL FEATURE; FAMILIAL DISEASE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE 46,XX; MENTAL DEFICIENCY; SHORT STATURE;

ADOLESCENT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; HUMANS; KARYOTYPING; MENTAL RETARDATION;

EID: 0030453087     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (9)