18p monosomy with midline defects and a de novo satellite identified by FISH

Annales de Genetique

Volumn 40, Issue 3, 1997, Pages 158-163

  Taine, L ^a   Goizet, C ^a   Wen, Z Q ^a   Chateil, J F ^a   Battin, J ^a   Saura, R ^a   Lacombe, D ^a  

^a HÔPITAL PELLEGRIN   (France)

Author keywords

18p monosomy; FISH; GH deficiency; Midline defects; Satellite

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 13P; CHROMOSOME 18P; CHROMOSOME TRANSLOCATION; DYSPLASIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GROWTH HORMONE DEFICIENCY; HUMAN; HUMAN CELL; HYPOPHYSIS; PARTIAL MONOSOMY; TOOTH MALFORMATION;

CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; DNA, SATELLITE; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MONOSOMY; TRANSLOCATION, GENETIC;

EID: 0030671506     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (260)