An unusual familial chromosome 9 "variant" with variable phenotype: characterization by CGH analysis.

Morphologie : bulletin de l'Association des anatomistes

Volumn 89, Issue 285, 2005, Pages 71-75

  Goumy, C ^a   Mihaescu, M ^a   Tchirkov, A ^a   Giollant, M ^a   Bonnet Dupeyron, M N ^a   Jaffray, J Y ^a   Geneix, A ^a   Perissel, B ^a   Francannet, C ^a   Boespflug Tanguy, O ^a   Vago, P ^a  

^a UNIVERSITÉ CLERMONT AUVERGNE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 9; CHROMOSOME ABERRATION; CONGENITAL MALFORMATION; FACE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC VARIABILITY; GENETICS; GROWTH DISORDER; HUMAN; LANGUAGE DISABILITY; MALE; PEDIGREE; PHENOTYPE;

CHILD; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 9; FACE; FEMALE; GROWTH DISORDERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LANGUAGE DISORDERS; MALE; PEDIGREE; PHENOTYPE; VARIATION (GENETICS);

EID: 24944588016     PISSN: 12860115     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1286-0115(05)83241-2     Document Type: Article

References (0)