Molecular and clinical examination of an Italian DEFECT 11 family

European Journal of Human Genetics

Volumn 7, Issue 5, 1999, Pages 579-584

  Wuyts, W ^a   Di Gennaro, G ^a   Bianco, F ^a   Wauters, J ^a   Morocutti, C ^a   Pierelli, F ^a   Bossuyt, P ^a   Van Hul, W ^a   Casali, C ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

Brain abnormalities; Chromosome 11; DEFECT 11; Deletion; FPP; Multiple exostoses

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CENTRAL NERVOUS SYSTEM MALFORMATION; CHROMOSOME 11P; CHROMOSOME DELETION; CONGENITAL DISORDER; DEFECT 11 SYNDROME; FAMILY STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; HEREDITARY MULTIPLE EXOSTOSIS; HUMAN; ITALY; MALE; PRIORITY JOURNAL; SKULL MALFORMATION;

ADULT; CENTRAL NERVOUS SYSTEM; CHROMOSOMES, HUMAN, PAIR 11; EXOSTOSES, MULTIPLE HEREDITARY; FEMALE; HUMANS; ITALY; MAGNETIC RESONANCE IMAGING; MALE; PARIETAL BONE; PEDIGREE; SEQUENCE DELETION; SYNDROME;

EID: 0032787808     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200339     Document Type: Article

References (26)